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STANDARD SET 374 F

APPLIED MEDICAL RESOURCES CORPORATION · Model GK249 · UDI-DI 20607915133430

FHFGCJFZPMDM Prescription
3
510(k) clearances
36
Adverse events (1 deaths)
0
Recalls
12
Facilities

Description

Kit Contains: CFF73, 12x100 Kii Fios ADVFIX 6/BX CFS22, 12x100 Kii SLEEVE ADVFIX 12/BX C6001, 5mmX33cm PROB/VALV DUAL BAG 12/BX CA090, DIRECT DRIVE LCA 3/BX

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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.