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Endolaser 120

FDA UDI

Class II (US FDA UDI)

by Enraf-Nonius B.V.

Identity

Trade Name
Endolaser 120 FDA UDI
Generic Name
Musculoskeletal/physical therapy laser, professional FDA UDI
Device Name
Device for low level laser therapy FDA UDI
Model / Reference
1633931 FDA UDI
Description
Device for low level laser therapy FDA UDI

Identifiers

Primary DI / UDI-DI
08720618311153 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Musculoskeletal/physical therapy laser, professional 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

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

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: Musculoskeletal/physical therapy laser, professional

Endolaser 120 by Enraf-Nonius B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Musculoskeletal/physical therapy laser, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Enraf-Nonius B.V.

Sources (1)

  • FDA UDI e7598f7a-607b-40cf-8f00-b8c974e2dcc9 34 fields · synced May 30, 2026