Home › devemed GmbH › devemed
devemed
devemed GmbH · Model 2422 · UDI-DI 04061644005154
KCB
Prescription
1
510(k) clearances
8
Adverse events
1
Recalls
109
Facilities
Description
Suction cannula Ø 4.0mm | 19.0cm front: Ø 4.0/3.0mm; back: Ø 6.0/5.0mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-04-08 | MEDLINE INDUSTRIES, LP - Northfield | Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma |
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.
