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Topsuper Med TPYZC-3

by Topsuper Med, Inc.

Topsuper Med TPYZC-3 is a Class II device made by Topsuper Med, Inc., listed in FDA GUDID since 4 Dec 2023 (UDI-DI 00197644720941), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00197644720941 UDI-DI Date4 Dec 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Topsuper Med
Generic name
Haemorrhoid ligation set
Model / reference
TPYZC-3
Primary DI / UDI-DI
00197644720941
FDA product code
FHN
GMDN term
Haemorrhoid ligation set
Device class
Class II
Regulation number
876.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Haemorrhoid ligation set

Similar devices

Other devices filed under FDA product code FHN (Ligator, Hemorrhoidal).

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)