Data / Medical devices / United States / Global Blood Resources, LLC
Global Blood Resources, LLC: FDA-registered device maker in Windsor, CT, United States, 2 510(k) clearances
Global Blood Resources, LLC is registered with the FDA (registration 3004080795) in Windsor, CT, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 26, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004080795
- Address
- 998 Windsor Ave, Windsor, CT, United States, 06095
- Owner or operator
- GLOBAL BLOOD RESOURCES, LLC (9056015)
- Roles
- Specification developer
- First device listed
- December 21, 2007
- Registered through
- 2026
- Brand names listed
- Hemobag, TS3 Tubing Set
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass | DWF | 2 | Specification developer | accessdata.fda.gov |
| Reservoir, Blood, Cardiopulmonary Bypass | DTN | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 26, 2003 | K031151 | TS3 TUBING SET | DWF | Substantially Equivalent | Global Blood Resources, LLC | accessdata.fda.gov |
| June 23, 2003 | K031150 | HEMOBAG, MODEL HBBSD2000 | DTN | Substantially Equivalent | Global Blood Resources, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Reservoir, Blood, Cardiopulmonary Bypass
- All makers of Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Updated June 26, 2003. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.