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KE011 SET URGENCIAS
APPLIED MEDICAL RESOURCES CORPORATION · Model GK222 · UDI-DI 20607915130712
3
510(k) clearances
36
Adverse events (1 deaths)
0
Recalls
12
Facilities
Description
Kit Contains: C2201, 120MM INSUFF NEEDLE XE, 20/BX CTF73, 12x100 Kii Fios ZTHR 6/BX CTB73, 12x100 Kii SH BLD ZTHR 6/BX CTF03, 5x100 Kii Fios Z-THR 6/BX C6001, 5mmX33cm PROB/VALV DUAL BAG 12/BX CA090, DIRECT DRIVE LCA 3/BX CD001, 10mm RETRIEVAL SYSTEM, 10/BX
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.
