Home › DELCON SRL › WELD B
WELD B
DELCON SRL · Model HWELD-B.DB.00G · UDI-DI 08033928530443
KSD
Prescription
1
510(k) clearances
10
Adverse events (1 deaths)
1
Recalls
18
Facilities
Description
Mobile tube sealer for medical PVC tubes
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-01-31 | Haemonetics Corporation | Battery pack may have exposed wire becoming hot |
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.