Skip to content

Alleset CP01220777PX01A

by GRI Medical & Electronic Technology Co., Ltd.

Alleset CP01220777PX01A is a Class I device made by GRI Medical & Electronic Technology Co., Ltd., listed in FDA GUDID since 28 Oct 2026 (UDI-DI 16942748496336), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number16942748496336 UDI-DI Date28 Oct 2026ListedStatusListed 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  • Withdrawn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
Alleset
Generic name
General surgical procedure kit, non-medicated, single-use
Model / reference
CP01220777PX01A
Primary DI / UDI-DI
16942748496336
FDA product code
PZG
GMDN term
General surgical procedure kit, non-medicated, single-use
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution

Other devices from GRI Medical & Electronic Technology Co., Ltd.

See all devices from GRI Medical & Electronic Technology Co., Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)