Dr David H Kramer, MD - Medicare Diagnostic Radiology in Lancaster, PA

Dr David H Kramer, MD is a medicare enrolled "Radiology - Diagnostic Radiology" physician in Lancaster, Pennsylvania. He went to Temple University School Of Medicine and graduated in 1992 and has 32 years of diverse experience with area of expertise as Diagnostic Radiology. He is a member of the group practice Lancaster Radiology Associates, Ltd., University Of Penn - Medical Group and his current practice location is 555 N Duke St, Lancaster, Pennsylvania. You can reach out to his office (for appointments etc.) via phone at (717) 544-4900.

Dr David H Kramer is licensed to practice in New Jersey (license number 25MA06686200) and he also participates in the medicare program. He accepts medicare assignments (which means he accepts the Medicare-approved amount; you will not be billed for any more than the Medicare deductible and coinsurance) and his NPI Number is 1205835949.

Contact Information

Dr David H Kramer, MD
555 N Duke St,
Lancaster, PA 17602-2250
(717) 544-4900
Not Available



Physician's Profile

Full NameDr David H Kramer
GenderMale
SpecialityDiagnostic Radiology
Experience32 Years
Location555 N Duke St, Lancaster, Pennsylvania
Accepts Medicare AssignmentsYes. He accepts the Medicare-approved amount; you will not be billed for any more than the Medicare deductible and coinsurance.
  Medical Education and Training:
  • Dr David H Kramer attended and graduated from Temple University School Of Medicine in 1992
  NPI Data:
  • NPI Number: 1205835949
  • Provider Enumeration Date: 07/15/2005
  • Last Update Date: 12/04/2023
  Medicare PECOS Information:
  • PECOS PAC ID: 7719918515
  • Enrollment ID: I20230628004073

Medical Identifiers

Medical identifiers for Dr David H Kramer such as npi, medicare ID, medicare PIN, medicaid, etc.
IdentifierTypeStateIssuer
1205835949NPI-NPPES
2118858OtherUNITED HEALTHCARE
300114883OtherRAILROAD MEDICARE
2531299OtherAETNA
A3738029OtherOXFORD HEALTH
KR1313821OtherPREMIER BLUE
2007103000OtherAMERIHEALTH
KR1313821OtherHIGHMARK PA BLUE SHIELD

Medical Taxonomies and Licenses

TaxonomyTypeLicense (State)Status
2085R0202XRadiology - Diagnostic Radiology 25MA06686200 (New Jersey)Primary

Medical Facilities Affiliation

Facility NameLocationFacility Type
Lancaster General HospitalLancaster, PAHospital
Chester County HospitalWest chester, PAHospital

Group Practice Association

Group Practice NameGroup PECOS PAC IDNo. of Members
Lancaster Radiology Associates, Ltd.064826752638
University Of Penn - Medical Group62047309553031

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› Verified 2 days ago

Medicare Reassignments

Some practitioners may not bill the customers directly but medicare billing happens through clinics / group practice / hospitals where the provider works. Medicare reassignment of benefits is a mechanism by which practitioners allow third parties to bill and receive payment for medicare services performed by them. Dr David H Kramer allows following entities to bill medicare on his behalf.
Entity NameLancaster Radiology Associates, Ltd.
Entity TypePart B Supplier - Clinic/group Practice
Entity IdentifiersNPI Number: 1669427100
PECOS PAC ID: 0648267526
Enrollment ID: O20040430000890

News Archive

GUMC study examines patients' most preferred methods for receiving common medical test results

The results of common medical tests are sometimes delivered to patients by email, letters or voice mail, but are these the most preferred methods? According to one of the first studies to look at this question, the answer is no.

Research shows brain cells move like a two-stroke engine

Following the often-quoted advice of Yogi Berra — "You can observe a lot by just watching" — Rockefeller University scientists show that nerve cells in the developing brains of humans and other mammals move in a two-part "step" led by a structure within the cell called the centrosome.

MUSC researchers show how non-coding RNA promotes tumor formation

A mechanism that pushes a certain gene to produce a non-coding form of RNA instead of its protein-coding alternative can promote the growth of cancer, report researchers at the Medical University of South Carolina in an article published online ahead of print on August 21, 2017 by Nature Cell Biology.

Fused indolines made by asymmetrical carbon–carbon coupling

Many drugs are based on natural substances. Because it is usually difficult, if not impossible, to isolate these in sufficient quantities from plants or microorganisms, they must be synthesized in the laboratory. This requires linking carbon atoms – with the right spatial orientation (stereochemistry) relative to each other. In the journal Angewandte Chemie, E. Peter Kündig and a team from the University of Geneva (Switzerland) have now introduced a palladium-catalyzed synthesis that allows them to produce indoline derivatives with the correct spatial arrangement.

Hormonal therapy may protect women's ovaries, increase chances of pregnancy after breast cancer treatment

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› Verified 2 days ago

Entity NameMri Group, Llp
Entity TypePart B Supplier - Clinic/group Practice
Entity IdentifiersNPI Number: 1518129196
PECOS PAC ID: 3779554464
Enrollment ID: O20080729000341

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The results of common medical tests are sometimes delivered to patients by email, letters or voice mail, but are these the most preferred methods? According to one of the first studies to look at this question, the answer is no.

Research shows brain cells move like a two-stroke engine

Following the often-quoted advice of Yogi Berra — "You can observe a lot by just watching" — Rockefeller University scientists show that nerve cells in the developing brains of humans and other mammals move in a two-part "step" led by a structure within the cell called the centrosome.

MUSC researchers show how non-coding RNA promotes tumor formation

A mechanism that pushes a certain gene to produce a non-coding form of RNA instead of its protein-coding alternative can promote the growth of cancer, report researchers at the Medical University of South Carolina in an article published online ahead of print on August 21, 2017 by Nature Cell Biology.

Fused indolines made by asymmetrical carbon–carbon coupling

Many drugs are based on natural substances. Because it is usually difficult, if not impossible, to isolate these in sufficient quantities from plants or microorganisms, they must be synthesized in the laboratory. This requires linking carbon atoms – with the right spatial orientation (stereochemistry) relative to each other. In the journal Angewandte Chemie, E. Peter Kündig and a team from the University of Geneva (Switzerland) have now introduced a palladium-catalyzed synthesis that allows them to produce indoline derivatives with the correct spatial arrangement.

Hormonal therapy may protect women's ovaries, increase chances of pregnancy after breast cancer treatment

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Read more Medical News

› Verified 2 days ago

Entity NameUniversity Of Penn - Medical Group
Entity TypePart B Supplier - Clinic/group Practice
Entity IdentifiersNPI Number: 1235527342
PECOS PAC ID: 6204730955
Enrollment ID: O20141111000091

News Archive

GUMC study examines patients' most preferred methods for receiving common medical test results

The results of common medical tests are sometimes delivered to patients by email, letters or voice mail, but are these the most preferred methods? According to one of the first studies to look at this question, the answer is no.

Research shows brain cells move like a two-stroke engine

Following the often-quoted advice of Yogi Berra — "You can observe a lot by just watching" — Rockefeller University scientists show that nerve cells in the developing brains of humans and other mammals move in a two-part "step" led by a structure within the cell called the centrosome.

MUSC researchers show how non-coding RNA promotes tumor formation

A mechanism that pushes a certain gene to produce a non-coding form of RNA instead of its protein-coding alternative can promote the growth of cancer, report researchers at the Medical University of South Carolina in an article published online ahead of print on August 21, 2017 by Nature Cell Biology.

Fused indolines made by asymmetrical carbon–carbon coupling

Many drugs are based on natural substances. Because it is usually difficult, if not impossible, to isolate these in sufficient quantities from plants or microorganisms, they must be synthesized in the laboratory. This requires linking carbon atoms – with the right spatial orientation (stereochemistry) relative to each other. In the journal Angewandte Chemie, E. Peter Kündig and a team from the University of Geneva (Switzerland) have now introduced a palladium-catalyzed synthesis that allows them to produce indoline derivatives with the correct spatial arrangement.

Hormonal therapy may protect women's ovaries, increase chances of pregnancy after breast cancer treatment

Young women undergoing chemotherapy for breast cancer may be more likely to remain fertile if they also receive hormonal treatment, according to new research presented to the 2015 European Cancer Congress on Monday and published simultaneously in Annals of Oncology.

Read more Medical News

› Verified 2 days ago

Medicare Part D Prescriber Enrollment

Any physician or other eligible professional who prescribes Part D drugs must either enroll in the Medicare program or opt out in order to prescribe drugs to their patients with Part D prescription drug benefit plans. Dr David H Kramer is enrolled with medicare and thus, if eligible, can prescribe medicare part D drugs to patients with medicare part D benefits.

Mailing Address and Practice Location

Mailing AddressPractice Location Address
Dr David H Kramer, MD
Po Box 4216,
Lancaster, PA 17604-4216

Ph: (717) 394-6028
Dr David H Kramer, MD
555 N Duke St,
Lancaster, PA 17602-2250

Ph: (717) 544-4900

News Archive

GUMC study examines patients' most preferred methods for receiving common medical test results

The results of common medical tests are sometimes delivered to patients by email, letters or voice mail, but are these the most preferred methods? According to one of the first studies to look at this question, the answer is no.

Research shows brain cells move like a two-stroke engine

Following the often-quoted advice of Yogi Berra — "You can observe a lot by just watching" — Rockefeller University scientists show that nerve cells in the developing brains of humans and other mammals move in a two-part "step" led by a structure within the cell called the centrosome.

MUSC researchers show how non-coding RNA promotes tumor formation

A mechanism that pushes a certain gene to produce a non-coding form of RNA instead of its protein-coding alternative can promote the growth of cancer, report researchers at the Medical University of South Carolina in an article published online ahead of print on August 21, 2017 by Nature Cell Biology.

Fused indolines made by asymmetrical carbon–carbon coupling

Many drugs are based on natural substances. Because it is usually difficult, if not impossible, to isolate these in sufficient quantities from plants or microorganisms, they must be synthesized in the laboratory. This requires linking carbon atoms – with the right spatial orientation (stereochemistry) relative to each other. In the journal Angewandte Chemie, E. Peter Kündig and a team from the University of Geneva (Switzerland) have now introduced a palladium-catalyzed synthesis that allows them to produce indoline derivatives with the correct spatial arrangement.

Hormonal therapy may protect women's ovaries, increase chances of pregnancy after breast cancer treatment

Young women undergoing chemotherapy for breast cancer may be more likely to remain fertile if they also receive hormonal treatment, according to new research presented to the 2015 European Cancer Congress on Monday and published simultaneously in Annals of Oncology.

Read more News

› Verified 2 days ago


Radiology Doctors in Lancaster, PA

Dr. Matthew Jason Winfeld, M.D.
Radiology
Medicare: Accepting Medicare Assignments
Practice Location: 555 N Duke St, Lancaster, PA 17602
Phone: 717-544-4900    Fax: 717-544-5907
Patrick Weybright,
Radiology
Medicare: Accepting Medicare Assignments
Practice Location: 555 N Duke St, Suite 3950, Lancaster, PA 17602
Phone: 717-299-4173    
Paul T Collura, MD
Radiology
Medicare: Not Enrolled in Medicare
Practice Location: 250 College Ave, Lancaster, PA 17603
Phone: 717-735-8199    
Steven A Morales, M.D.
Radiology
Medicare: Medicare Enrolled
Practice Location: 555 N Duke St, Lancaster, PA 17602
Phone: 717-544-4900    Fax: 717-544-5907
Dr. John Briguglio, M.D.
Radiology
Medicare: Accepting Medicare Assignments
Practice Location: 555 N Duke St, Lancaster, PA 17602
Phone: 717-394-6028    Fax: 717-394-9223
Alan Alexander, MD
Radiology
Medicare: Not Enrolled in Medicare
Practice Location: 250 College Ave, Lancaster, PA 17603
Phone: 717-735-8188    
Dr. Margarita M Shultz, M.D.
Radiology
Medicare: Not Enrolled in Medicare
Practice Location: 1300 Millersville Pike, Lancaster, PA 17603
Phone: 717-393-5892    Fax: 717-393-3774

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