Home › Dermapac Inc. › Dermapac, Inc.
Dermapac, Inc.
Dermapac Inc. · Model 8801 · UDI-DI 10810102271355
10
510(k) clearances
518
Adverse events (14 deaths)
1
Recalls
232
Facilities
Description
Retention Booties ID 1/8" wall 1/32" OD 3/16" 3" long 4/pk
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-08-10 | A M Systems Inc | Some of the Disposable Smooth Interior Tubing may pull apart when stretched. |
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 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.