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Emsrun PZBB0005-3

by Wuxi Emsrun Technology Co., Ltd.

Emsrun PZBB0005-3 is a Class I device made by Wuxi Emsrun Technology Co., Ltd., listed in FDA GUDID since 6 Dec 2022 (UDI-DI 06974567743332), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06974567743332 UDI-DI Date6 Dec 2022ListedStatusListed 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  • Withdrawn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
Emsrun
Generic name
Open surgical site internal light
Model / reference
PZBB0005-3
Primary DI / UDI-DI
06974567743332
FDA product code
KYT
GMDN term
Open surgical site internal light
Device class
Class I
Regulation number
880.6350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Open surgical site internal light

Other devices from Wuxi Emsrun Technology Co., Ltd.

See all devices from Wuxi Emsrun Technology Co., Ltd. →

Properties

  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (11, all answered No)