← Back to catalogue

LipoSense 25cm, 3mm Mercedes with Temp Sensor & Sensor Box

FDA UDI

Class II (US FDA UDI)

by Alma Lasers Ltd.

Identity

Trade Name
LipoSense 25cm, 3mm Mercedes with Temp Sensor & Sensor Box FDA UDI
Generic Name
General/multiple surgical diode laser system FDA UDI
Device Name
A temperature sensing thermistor to the cannula to be use during laser lipolysis procedures. FDA UDI
Model / Reference
1 FDA UDI
Description
A temperature sensing thermistor to the cannula to be use during laser lipolysis procedures. FDA UDI

Identifiers

Catalog Number
AALS22112004 FDA UDI
Primary DI / UDI-DI
17290110120808 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
General/multiple surgical diode laser system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General/multiple surgical diode laser system

LipoSense 25cm, 3mm Mercedes with Temp Sensor & Sensor Box by Alma Lasers Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General/multiple surgical diode laser system.

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
Alma Lasers Ltd.

Sources (1)

  • FDA UDI e64c1d78-e6a3-4b39-9bba-cf95302209c1 34 fields · synced May 30, 2026