CARTER BLOODCARE

FDA Device Registration & Listing · Bedford, TX, US · Registration 3002603147

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3002603147
FEI Number
3002603147
Entity Name
CARTER BLOODCARE
City/State/Country
Bedford, TX, US
Establishment Address
2205 Highway 121, Bedford, TX 76021, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Carter Bloodcare (Owner Number: 10055698)
Owner / Operator Contact Address
2205 Highway 121, Bedford, TX 76021, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

iWeBB electronic Laboratory Information System eLIS iWeBB eLIS electronic Laboratory Infomation System BBIMS Blood Bank Information Management System (BBIMS) Blood Bank Information Management System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MMH Blood Establishment Computer Software And Accessories Hematology Class 2 864.9165 2020-12-09
MMH Blood Establishment Computer Software And Accessories Hematology Class 2 864.9165 2024-07-30

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Carter Bloodcare
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3009166014 KEDRION S.P.A. Barga (Castelvecchio Pascoli) Lucca, IT
3006129391 WellSky Corporation. - Headquarters Overland Park, KS, US
3017199812 GPI USA, INC. Houston, TX, US
3020696801 CieloWorks Austin, TX, US
1058332 SCC SOFT COMPUTER CLEARWATER, FL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3002603147. Last updated year: 2026. Please use registration number 3002603147 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.