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CARBO

Wujiang City ShenLing Medical Device Co.,Ltd · Model CT1-3605 · UDI-DI 06973169040887

MQX
1
510(k) clearances
13
Adverse events
1
Recalls
72
Facilities

Description

Classic Series CT1 Blister Pack with tube

Recalls

DateFirmReason
2007-11-28Marknew ProductsMarketed without 510(k)

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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.