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Ltu-904

FDA UDI

Class II (US FDA UDI)

by Medical Manufacturers Pty Ltd

Identity

Trade Name
LTU-904 FDA UDI
Generic Name
Musculoskeletal/physical therapy laser, home-use FDA UDI
Device Name
Low Level Laser Therapy Device FDA UDI
Model / Reference
LTU-904 FDA UDI
Description
Low Level Laser Therapy Device FDA UDI

Identifiers

Catalog Number
FG00002 FDA UDI
Primary DI / UDI-DI
09352877000135 FDA UDI
FDA Product Code
NZY FDA UDI
GMDN Term
Musculoskeletal/physical therapy laser, home-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5500 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

Category: Musculoskeletal/physical therapy laser, home-use

Ltu-904 by Medical Manufacturers Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Musculoskeletal/physical therapy laser, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Manufacturers Pty Ltd

Sources (1)

  • FDA UDI 40e4c7dd-0c94-4142-adfc-d2bf9cbfe5a3 34 fields · synced Jun 8, 2026