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Na AG-5104-2300-090

by Hangzhou AGS MedTech Co., Ltd.

Listed FDA GUDID listing, not in commercial distribution

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 Number06959664903001 UDI-DI Date28 May 2018ListedStatusListed GUDID: not 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  • Withdrawn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
Gastrointestinal endoscopic clip, short-term
Model / Ref / Catalog
AG-5104-2300-090, AG6.510E.0493.000.Z
Primary DI / UDI-DI
06959664903001
510(k) Number
FDA Product Code
PKL
GMDN Term
Gastrointestinal endoscopic clip, short-term
Device Class
Class II
Regulation Number
876.4400
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Conditional

Related devices

Category: Gastrointestinal endoscopic clip, short-term

Cleared under the same submission (K172727)

Show all (12)

Similar devices

Also classified as Gastrointestinal endoscopic clip, short-term.

Other devices from Hangzhou AGS MedTech Co., Ltd.

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Properties

  • Sterile
  • Single Use
  • Contains Latex
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

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