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Barkey plasmatherm C&G

Barkey GmbH & Co. KG · Model US-C&G · UDI-DI 04059201001817

KZL Prescription
4
510(k) clearances
828
Adverse events (8 deaths)
0
Recalls
13
Facilities

Description

Thawing and warming device for frozen plasma (FFP, PF24 ,AHF), Whole Blood, RBC and IV solution

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.