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Liger Medical

by Liger Medical

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860005151004 UDI-DI Date5 May 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Electrocautery system generator, battery-powered
Model / Reference
IRIS Thermocoagulator and Digital Colposcope Unit
Primary DI / UDI-DI
00860005151004
510(k) Number
FDA Product Code
HGI, PTZ
GMDN Term
Electrocautery system generator, battery-powered
Device Class
Class II
Regulation Number
884.4120, 884.1630
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Liger Medical

See all devices from Liger Medical →

Properties

  • Prescription Use
  • Serial Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No