FDA Device Intelligence
Home › Coloplast A/S › Coloplast

Coloplast

Coloplast A/S · Model 14015 · UDI-DI 00762123049518

GBQ Prescription
8
510(k) clearances
75
Adverse events (1 deaths)
1
Recalls
25
Facilities

Description

Coloplast / Coloplast Drain Port.

Recalls

DateFirmReason
2015-06-29Merit Medical Systems, Inc.Merit Medical Systems, Inc. is voluntarily conducting a recall due to a potential discrepancy between the unit labeling of the Merit ReSolve Drainage Catheters and the actual devic

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 docs
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.