Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003374183

FEI Number

3003374183

Entity Name

CBR SYSTEMS, INC.

City/State/Country

Tucson, AZ, US

Establishment Address

6550 S BAY COLONY DR STE 160, Tucson, AZ 85756, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

CBR Systems, Inc (Owner Number: 10047651)

Owner / Operator Contact Address

11915 La Grange Ave, Los Angeles, CA 90025, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CBR Newborn Stem Cell Collection Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MYK	Kit, Cord Blood Collection	Unknown	Class N	N/A	2014-10-16

Official Correspondent

Tamanna Patel

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CBR Systems, Inc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003374183. Last updated year: 2026. Please use registration number 3003374183 when referencing this establishment in official correspondence.