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Multi Sealer MS 1000

Sarstedt Aktiengesellschaft & Co.KG · Model 87.7708.800 · UDI-DI 04038917341608

KSD
1
510(k) clearances
10
Adverse events (1 deaths)
1
Recalls
18
Facilities

Recalls

DateFirmReason
2011-01-31Haemonetics CorporationBattery pack may have exposed wire becoming hot

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.