FDA Device Intelligence
Home › EXMOOR PLASTICS LIMITED › EXMOOR

EXMOOR

EXMOOR PLASTICS LIMITED · Model US5-150SF · UDI-DI 05060180258689

JZF
5
510(k) clearances
41
Adverse events
0
Recalls
145
Facilities

Description

Suction Tube

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.