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COMPACT 2

PROTEC GmbH & Co. KG · Model 1190 · UDI-DI 04260502640005

IXW
10
510(k) clearances
45
Adverse events
1
Recalls
2
Facilities

Description

Darkroom automated x-ray film processor

Recalls

DateFirmReason
2016-04-01Fujifilm Medical Systems U.S.A., Inc.Reports of failure of the device's power supply.

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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.