FDA Device Intelligence
Home › Phillips-Medisize A/S › myBETAapp

myBETAapp

Phillips-Medisize A/S · Model iOS (Mobile App) · UDI-DI 05713495000053

NXQ
2
510(k) clearances
7
Adverse events
1
Recalls
61
Facilities

Recalls

DateFirmReason
2006-08-02Eatonform IncCertain lots of packet components of the firm's Doc-U-Dose Prescription Management System are separating from the paper along the sealed seam at the bottom of the packets causing t

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.