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Na AG-55501-1800-135-13

by Hangzhou AGS MedTech Co., Ltd.

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06959664919200 UDI-DI Date16 Jul 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  • Withdrawn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

Generic Name
Gastrointestinal endoscopic clip, short-term
Model / Reference
AG-55501-1800-135-13
Primary DI / UDI-DI
06959664919200
FDA Product Code
PKL
GMDN Term
Gastrointestinal endoscopic clip, short-term
Device Class
Class II
Regulation Number
876.4400
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Other devices from Hangzhou AGS MedTech Co., Ltd.

See all devices from Hangzhou AGS MedTech Co., Ltd. →

Properties

  • Sterile
  • Single Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No