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Verju

FDA UDI

Class II (US FDA UDI)

by Erchonia Corporation

Identity

Trade Name
Verju FDA UDI
Generic Name
Low-intensity laser fat liquefaction system FDA UDI
Device Name
AESTHETIC - Floor Model Low Level Laser - 6 diodes 532nm 17mW FDA UDI
Model / Reference
CLS FDA UDI
Description
AESTHETIC - Floor Model Low Level Laser - 6 diodes 532nm 17mW FDA UDI

Identifiers

Catalog Number
CLS FDA UDI
Primary DI / UDI-DI
00858985006070 FDA UDI
FDA Product Code
OLI FDA UDI
GMDN Term
Low-intensity laser fat liquefaction system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Low-intensity laser fat liquefaction system

Verju by Erchonia Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Low-intensity laser fat liquefaction system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 11f47809-d90f-471b-91f4-38c674a38b7f 35 fields · synced Jun 9, 2026