FDA Device Intelligence
HomeBeaver-Visitec International, Inc. › Visitec®

Visitec®

Beaver-Visitec International, Inc. · Model 581630 · UDI-DI 30886158002568

HNY
10
510(k) clearances
30
Adverse events
0
Recalls
78
Facilities

Description

CYSTOTOME IRRIGATING 30G 5/8IN (10/SP)

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.