KES

GUDID 06971513121022

Beijing KES Biology Technology Co.,Ltd.

Intense pulsed light skin surface treatment system
Primary Device ID06971513121022
NIH Device Record Keyd2931e31-9d7b-4791-9935-a517cb10cb38
Commercial Distribution StatusIn Commercial Distribution
Brand NameKES
Version Model NumberMED-230
Company DUNS525608013
Company NameBeijing KES Biology Technology 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
GS106971513121022 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

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 Date2020-07-21
Device Publish Date2020-07-13

On-Brand Devices [KES]

06971513121022MED-230
06971513121039MED-810A
06971513121015MED-210
06971513121046MED-808

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