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Revolve Advanced Adipose System

FDA UDI

Class II (US FDA UDI)

by Lifecell Corp

Identity

Trade Name
Revolve Advanced Adipose System FDA UDI
Generic Name
Surgical suction system collection container, single-use FDA UDI
Model / Reference
RV0001 FDA UDI

Identifiers

Primary DI / UDI-DI
M328RV000106 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

Yes

FDA UDI

Category: Surgical suction system collection container, single-use

Revolve 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

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Manufacturer

Manufacturer
Lifecell Corp

Sources (1)

  • FDA UDI 6381a71f-8c17-4848-9470-c9bab15ceb62 33 fields · synced May 30, 2026