Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004080795

FEI Number

3004080795

Entity Name

GLOBAL BLOOD RESOURCES, LLC

City/State/Country

WINDSOR, CT, US

Establishment Address

998 Windsor Ave, WINDSOR, CT 06095, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

GLOBAL BLOOD RESOURCES, LLC (Owner Number: 9056015)

Owner / Operator Contact Address

998 WINDSOR AVE., --, Windsor, CT 06095, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K031150

PMA Number

N/A

All Registered Proprietary Names

TS3 Tubing Set Hemobag

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DWF	Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass	Cardiovascular	Class 2	870.4210	2007-12-21
DTN	Reservoir, Blood, Cardiopulmonary Bypass	Cardiovascular	Class 2	870.4400	2007-12-21

Official Correspondent

KEITH SAMOLYK

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GLOBAL BLOOD RESOURCES, LLC

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K832124	Med-West, Inc.	CPC, COUBLE LUMEN CARDIOPLEGIA-AIR ASPI	1983-08-12
K162500	Spyder Medical	Ostial Sprit Cannulae	2017-01-12
K862357	3M Health Care, Sarns	MODIFIED CARDIOTOMY RESERVOIR 5M1470	1986-08-19

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0003-2022	Medtronic Perfusion Systems	2	Medtronic Bio-Medicus Insertion Kits, Model number 96553, Pediatric Insertion Kit, Sterile; and Model number 96551, Venous Insertion Kit, Sterile.
Z-0021-2018	OriGen Biomedical, Inc.	2	The OriGen Reinforced Dual Lumen catheter (RDLC) is a duel lumen catheter with a wire reinforcement layer on the tip of the device. A thin sheath is used to cover and secure the wire layer and is heat shrunk into a permanent position.

Similar Registrations

Registration Number	Establishment Name	Location
3038776570	INVOSURG INC	Canton, MA, US
3009380063	Medtronic Distribution Center	Memphis, TN, US
2916596	THORATEC CORP.	PLEASANTON, CA, US
1836324	Rose Medical	Grand Rapids, MI, US
3019807891	CENTERPIECE S. DE R.L DE C.V (sterilization site)	Tijuana Baja California, MX

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004080795. Last updated year: 2026. Please use registration number 3004080795 when referencing this establishment in official correspondence.