Home › B BRAUN SURGICAL SA › Monomax
Monomax
B BRAUN SURGICAL SA · Model B9941125 · UDI-DI 04046963989415
NWJ
Prescription
9
510(k) clearances
92
Adverse events
1
Recalls
3
Facilities
Description
MONOMAX VLT 1 (4) 90CM HR48 USA (M)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-02-08 | Tornier, Inc | Data has shown that degradation of a raw material used in Phantom Fiber may occur more quickly than expected if improperly stored. This may impact the shelf-life of the product wh |
Query this across every FDA database — by API.
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.