FDA Device Intelligence
Home › Mölnlycke Health Care AB › Mepiform®

Mepiform®

Mölnlycke Health Care AB · Model 293600 · UDI-DI 07332430998880

MDA
10
510(k) clearances
51
Adverse events (1 deaths)
0
Recalls
193
Facilities

Description

Mepiform 4x30cm non sterile

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.