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T-Shape 2

FDA UDI

Class II (US FDA UDI)

by B&M Srl Marketing Nel Benessere

Identity

Trade Name
T-SHAPE 2 FDA UDI
Generic Name
Multi-modality skin/body contouring system FDA UDI
Model / Reference
T-SHAPE 2 FDA UDI

Identifiers

Primary DI / UDI-DI
08053782383283 FDA UDI
510(k) Number
K231092 FDA UDI
FDA Product Code
NUV FDA UDI
PBX FDA UDI
GMDN Term
Multi-modality skin/body contouring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
878.4400 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: Multi-modality skin/body contouring system

T-Shape 2 by B&M Srl Marketing Nel Benessere — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality skin/body contouring system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dd6f340f-b7f4-439c-89bb-2a6bc6efe4e2 33 fields · synced Jun 1, 2026