Globalipl

GUDID 06973494935001

BEIJING GLOBALIPL DEVELOPMENT CO., LTD.

Intense pulsed light skin surface treatment system
Primary Device ID06973494935001
NIH Device Record Key46d13879-ebd4-42f0-a6bf-4c4f83f4ba60
Commercial Distribution StatusIn Commercial Distribution
Brand NameGlobalipl
Version Model NumberUS500
Company DUNS544936742
Company NameBEIJING GLOBALIPL DEVELOPMENT CO., LTD.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106973494935001 [Primary]

FDA Product Code

ONFPowered Light Based Non-Laser Surgical Instrument With Thermal Effect

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-08-24
Device Publish Date2022-08-16

On-Brand Devices [Globalipl]

06973494934196US419
06973494938019US800N
06973494938002US800
06973494935001US500
06973494934509US450

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