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MedLED

FDA UDI

Class I (US FDA UDI)

by Riverpoint Medical Llc

Identity

Trade Name
MedLED FDA UDI
Generic Name
Head-worn lamp FDA UDI
Device Name
Wall Mount FDA UDI
Model / Reference
M-90711 FDA UDI
Description
Wall Mount FDA UDI

Identifiers

Primary DI / UDI-DI
00840277404183 FDA UDI
FDA Product Code
HPP FDA UDI
GMDN Term
Head-worn lamp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4335 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: Head-worn lamp

MedLED by Riverpoint Medical Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Head-worn lamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a73f9ac3-26a7-4703-b9e5-358ee30f33f6 33 fields · synced May 29, 2026