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Vibrasat Pro Console

FDA UDI

Class II (US FDA UDI)

by Möller Medical GmbH

Identity

Trade Name
Vibrasat Pro Console FDA UDI
Generic Name
Liposuction system FDA UDI
Device Name
The vibrating drive system 'Vibrasat Pro' is used to oscillate cannulas to support the hand movement of the user. FDA UDI
Model / Reference
00003921 FDA UDI
Description
The vibrating drive system 'Vibrasat Pro' is used to oscillate cannulas to support the hand movement of the user. FDA UDI

Identifiers

Catalog Number
00003920 FDA UDI
Primary DI / UDI-DI
04260277178055 FDA UDI
510(k) Number
K053451 FDA UDI
FDA Product Code
QPB FDA UDI
GMDN Term
Liposuction system 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Liposuction system

Vibrasat Pro Console by Möller Medical GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liposuction system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 967e01af-e6cd-4f8c-a3b3-ce1d265089ee 35 fields · synced Jun 9, 2026