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Dryswab
MEDICAL WIRE & EQUIPMENT CO.(BATH)LIMITED · Model N/a · UDI-DI 05060259073137
4
510(k) clearances
39
Adverse events
1
Recalls
134
Facilities
Description
Dryswab-Straight aluminium wire, peel pouch, Dacron
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-28 | Neilmed Pharmaceuticals Inc | Due to nasal spray stability failure for bioburden. |
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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.