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Woodpecker LED.m

by Guilin Woodpecker Medical Instrument Co., Ltd. 2 variants

Woodpecker LED.m is a Class II device made by Guilin Woodpecker Medical Instrument Co., Ltd., listed in FDA GUDID since 10 Sep 2016 (UDI-DI 06944843602172), 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 Number06944843602172 UDI-DI Date10 Sep 2016ListedStatusListed 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  • Withdrawn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
Woodpecker
Generic name
Dental/surgical polymerization lamp
Model / reference
LED.M
Primary DI / UDI-DI
06944843602172
FDA product code
EBZ
GMDN term
Dental/surgical polymerization lamp
Device class
Class II
Regulation number
872.6070
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental/surgical polymerization lamp

Similar devices in this category

Other devices filed under Dental/surgical polymerization lamp.

Other devices from Guilin Woodpecker Medical Instrument Co., Ltd.

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Properties

  • Sterilise before use
  • Single use
  • Premarket exempt
  • Serial number
Other properties (11, all answered No)