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3M™ Unitek™

3M UNITEK CORPORATION · Model 803-003 · UDI-DI 00652221110053

ECP Prescription
0
510(k) clearances
1
Adverse events
0
Recalls
96
Facilities

Description

3M™ Unitek™ Single-Ended Ligature Director, 803-003, 1/Ea

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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.