FDA Device Intelligence
HomePhilipp Kirsch GmbH › Kirsch

Kirsch

Philipp Kirsch GmbH · Model BL 520 US PRO-ACTIVE · UDI-DI 04260688580331

KSE
4
510(k) clearances
383
Adverse events (3 deaths)
0
Recalls
38
Facilities

Description

Blood Bank Refrigerator BL 520 US PRO-ACTIVE

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.