Skip to content

Liger Medical EVA Pro Digital Colposcope

by Liger Medical

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07290016976106 UDI-DI Date2 Jun 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Liger Medical
Generic Name
Colposcope
Model / Reference
EVA Pro Digital Colposcope
Primary DI / UDI-DI
07290016976106
FDA Product Code
PTZ
GMDN Term
Colposcope
Device Class
Class II
Regulation Number
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
  • Premarket Exempt
  • Serial Number

Other properties (11)

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