← Back to catalogue

Revolve ENVI 600 Advanced Adipose System

FDA UDI

Class II (US FDA UDI)

by Lifecell Corp

Identity

Trade Name
Revolve ENVI 600 Advanced Adipose System FDA UDI
Generic Name
Surgical suction system collection container, single-use FDA UDI
Device Name
Tissue Processing System FDA UDI
Model / Reference
RV0001E600 FDA UDI
Description
Tissue Processing System FDA UDI

Identifiers

Catalog Number
RV0001E600 FDA UDI
Primary DI / UDI-DI
00818410012410 FDA UDI
FDA Product Code
MUU FDA UDI
QKL FDA UDI
GMDN Term
Surgical suction system collection container, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical suction system collection container, single-use

Revolve ENVI 600 Advanced Adipose System by Lifecell Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction system collection container, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Lifecell Corp

Sources (1)

  • FDA UDI 35130871-c9e9-4558-8804-1ec2d158fdc8 34 fields · synced Jun 8, 2026