Venus Bliss Max

FDA UDI

Class II (US FDA UDI)

by Venus Concept Inc.

Identity

Trade Name: Venus Bliss Max FDA UDI
Generic Name: Multi-modality skin surface treatment system FDA UDI
Model / Reference: BLMX0001 FDA UDI

Identifiers

Primary DI / UDI-DI: 00810060830987 FDA UDI
FDA Product Code: NGX FDA UDI
PBX FDA UDI
PKT FDA UDI
GMDN Term: Multi-modality skin surface treatment system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.5850 FDA UDI
878.4400 FDA UDI
878.5400 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multi-modality skin surface treatment system

Venus Bliss Max by Venus Concept Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Venus Concept Inc.

Sources (1)

FDA UDI a1e3cb3a-a1ab-44f2-be4e-5e4b5fe26cbc 32 fields · synced May 31, 2026