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Globalipl US800N

by Beijing Globalipl Development Co., Ltd.

Globalipl US800N is a dermatological carbon dioxide laser system (FDA Class II; FDA product code GEX, Powered Laser Surgical Instrument) made by Beijing Globalipl Development Co., Ltd., listed in FDA GUDID since 16 Aug 2022 (UDI-DI 06973494938019), 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 Number06973494938019 UDI-DI Date16 Aug 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  • Withdrawn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
Globalipl
Generic name
Dermatological carbon dioxide laser system
Model / reference
US800N
Primary DI / UDI-DI
06973494938019
FDA product code
GEX
GMDN term
Dermatological carbon dioxide laser system
Device class
Class II
Regulation number
878.4810
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GEX (Powered Laser Surgical Instrument).

Other devices from Beijing Globalipl Development Co., Ltd.

See all devices from Beijing Globalipl Development Co., Ltd. →

Properties

  • Serial number
  • Expiration date
Other properties (13, all answered No)