Venus Bliss Max

GUDID 00810060830987

Venus Concept Inc.

Multi-modality skin surface treatment system
Primary Device ID00810060830987
NIH Device Record Keya1e3cb3a-a1ab-44f2-be4e-5e4b5fe26cbc
Commercial Distribution StatusIn Commercial Distribution
Brand NameVenus Bliss Max
Version Model NumberBLMX0001
Company DUNS117333774
Company NameVenus Concept Inc.
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100810060830987 [Primary]

FDA Product Code

NGXStimulator, Muscle, Powered, For Muscle Conditioning

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-16
Device Publish Date2023-06-08

Devices Manufactured by Venus Concept Inc.

00810060831632 - ARTAS iX 2024-07-12
00810060830079 - ARTAS System2023-06-16
00810060830444 - Venus Bliss2023-06-16
00810060830574 - Venus Velocity2023-06-16
00810060830628 - Venus Viva 2023-06-16
00810060830680 - Venus Versa2023-06-16
00810060830826 - Venus Legacy (100V)2023-06-16
00810060830833 - Venus Legacy (120V)2023-06-16

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