FDA Device Intelligence
HomeDuPhaMed B.V. › Cefla

Cefla

DuPhaMed B.V. · Model CEF2062 · UDI-DI 08717228440274

EGZ
8
510(k) clearances
4
Adverse events
0
Recalls
128
Facilities

Description

X-Ray sensor holder Introduction Pack Size 2, content: 1x bitewing - UDI 08717228441042 1x posterior Upper Left / Lower Right - UDI 08717228441578 1x posterior Upper Right / Lower Left - UDI 08717228441585 1x periapical Upper Left / Lower Right - UDI 08717228441387 1x periapical Upper Right / Lower Left - UDI 08717228441394 1x endo Upper Left / Lower Right - UDI 08717228441219 1x endo Upper Right / Lower Left - UDI 08717228441226 1x positioning ring - UDI 08717228441028

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.