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Multisealer MS 500B
Sarstedt Aktiengesellschaft & Co.KG · Model 87.7708.860 · UDI-DI 04038917355315
1
510(k) clearances
10
Adverse events (1 deaths)
1
Recalls
18
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-01-31 | Haemonetics Corporation | Battery pack may have exposed wire becoming hot |
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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.
