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Alma TED System 120V 50/60HZ

FDA UDI

Class I (US FDA UDI)

by Alma Lasers Ltd.

Identity

Trade Name
Alma TED System 120V 50/60HZ FDA UDI
Generic Name
Physical therapy ultrasound system applicator, hand-held FDA UDI
Device Name
Alma TED System 120V 50/60HZ FDA UDI
Model / Reference
1 FDA UDI
Description
Alma TED System 120V 50/60HZ FDA UDI

Identifiers

Catalog Number
AATE16112101BA0001 FDA UDI
Primary DI / UDI-DI
07290110123567 FDA UDI
FDA Product Code
ISA FDA UDI
GMDN Term
Physical therapy ultrasound system applicator, hand-held FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5660 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Physical therapy ultrasound system applicator, hand-held

Alma TED System 120V 50/60HZ by Alma Lasers Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physical therapy ultrasound system applicator, hand-held.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alma Lasers Ltd.

Sources (1)

  • FDA UDI b21723ee-f33f-4ff1-855c-105e7b14543f 34 fields · synced May 30, 2026