FDA Device Intelligence
Home › Phadia AB › EliA RNP70 Well

EliA RNP70 Well

Phadia AB · Model DECC055110 · UDI-DI 07333066014623

LKO Prescription
10
510(k) clearances
0
Adverse events
1
Recalls
12
Facilities

Description

EliA RNP70 Well

Recalls

DateFirmReason
2016-10-21Euro Diagnostica ABIncorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin.

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.