FDA Device Intelligence
HomeSDI LIMITED › ULTRAMAT 2

ULTRAMAT 2

SDI LIMITED · Model 5546045 · UDI-DI 09336472005474

EFD
10
510(k) clearances
6
Adverse events
1
Recalls
32
Facilities

Description

ULTRAMAT 2MV US

Recalls

DateFirmReason
2026-07-20SDI LimitedPotential for electrical discharge from unit when unplugged.

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.