FDA Device Intelligence
Home › Spiggle & Theis Medizintechnik GmbH › Inflation device

Inflation device

Spiggle & Theis Medizintechnik GmbH · Model 2080-9030040-US · UDI-DI 04250676743473

PNZ Prescription
1
510(k) clearances
30
Adverse events
0
Recalls
16
Facilities

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.