Mrs Samantha Nunez, CAS - Counselor in Sacramento, CA

Mrs Samantha Nunez, CAS is a Counselor based in Sacramento, California. Mrs Samantha Nunez is licensed to practice in California (license number 340004BN) and her current practice location is 2515 48th Ave, Sacramento, California. She can be reached at her office (for appointments etc.) via phone at (916) 394-2328.

NPI number for Mrs Samantha Nunez is 1003056011 and her current mailing address is 2515 48th Ave, Sacramento, California. She does not participate in medicare program and thus does not accept medicare assignments. Her NPI Number is 1003056011.

Contact Information

Mrs Samantha Nunez, CAS
2515 48th Ave,
Sacramento, CA 95822-3810
(916) 394-2328
(916) 394-2457

Healthcare Provider's Profile

Full NameMrs Samantha Nunez
GenderFemale
SpecialityCounselor
Location2515 48th Ave, Sacramento, California
Accepts Medicare AssignmentsDoes not participate in Medicare Program. She may not accept medicare assignment.
  NPI Data:
  • NPI Number: 1003056011
  • Provider Enumeration Date: 03/03/2009
  • Last Update Date: 05/20/2013

Medical Identifiers

Medical identifiers for Mrs Samantha Nunez such as npi, medicare ID, medicare PIN, medicaid, etc.
IdentifierTypeStateIssuer
1003056011NPI-NPPES

Medical Taxonomies and Licenses

TaxonomyTypeLicense (State)Status
101Y00000XCounselor 340004BN (California)Primary

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. Mrs Samantha Nunez is NOT enrolled with medicare and thus cannot prescribe medicare part D drugs to patients with medicare part D benefits.

Mailing Address and Practice Location

Mailing AddressPractice Location Address
Mrs Samantha Nunez, CAS
2515 48th Ave,
Sacramento, CA 95822-3810

Ph: (916) 394-2328
Mrs Samantha Nunez, CAS
2515 48th Ave,
Sacramento, CA 95822-3810

Ph: (916) 394-2328

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Micronics, Inc., a medical device development company, today announced that the U.S. Food and Drug Administration has granted the company 510(k) clearance to market its ABORhCard, a qualitative in vitro test that provides a simultaneous determination of an individual's ABO blood group and Rh factor status. It is not for use for blood bank processing of blood products, for determining RHD status for the purpose of administration of Rh immunoglobulin, or for screening purposes prior to transfusion.

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› Verified 5 days ago


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