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DR. TENEWITZ

APPLIED MEDICAL RESOURCES CORPORATION · Model K2634 · UDI-DI 30607915133451

GEIHETGCJFZPMDM Prescription
10
510(k) clearances
119,015
Adverse events (469 deaths)
0
Recalls
858
Facilities

Description

Kit Contains: CA090, DIRECT DRIVE® LCA 3/BX CD001, 10mm RETRIEVAL SYSTEM, 10/BX CTS02, 5x100 Kii® SLEEVE ZTHR 12/BX CTF03, 5x100 Kii® Fios® Z-THR 6/BX CTF33, 11x100 Kii® Fios® ZTHR 6/BX CB030, 5mmx35cm EPIX® LAPA SCISSOR, 10/BX CY010, 5mmX35cm EPIX® LAPA DISSECT, 10/BX

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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.