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SAHARA

Transmed Medizintechnik GmbH & Co. KG · Model SAHARA-TSC 115V · UDI-DI 04028339720235

KZL

510(k) clearances

828

Adverse events (8 deaths)

Recalls

Facilities

Description

Thawing device for stem cell preparations

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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.