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Transform (T3 Applicator)

FDA UDI

Class II (US FDA UDI)

by Inmode MD , Ltd.

Identity

Trade Name
Transform (T3 Applicator) FDA UDI
Generic Name
Radio-frequency skin surface treatment system applicator FDA UDI
Device Name
Transform (T3 Applicator) FDA UDI
Model / Reference
AG609899A FDA UDI
Description
Transform (T3 Applicator) FDA UDI

Identifiers

Catalog Number
AG609899A FDA UDI
Primary DI / UDI-DI
07290016633689 FDA UDI
FDA Product Code
GZJ FDA UDI
IPF FDA UDI
PBX FDA UDI
GMDN Term
Radio-frequency skin surface treatment system applicator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 FDA UDI
890.5850 FDA UDI
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radio-frequency skin surface treatment system applicator

Transform (T3 Applicator) by Inmode MD , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radio-frequency skin surface treatment system applicator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Inmode MD , Ltd.

Sources (1)

  • FDA UDI b96b5bca-d28a-4685-81cb-f490a4533f30 36 fields · synced May 30, 2026