← Back to catalogue

Elmed Incorporated

FDA UDI

Class I (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED INCORPORATED FDA UDI
Generic Name
Head-worn lamp FDA UDI
Device Name
TRANSFORMER FOR LIST NO 9825 (HEADLIGHT), 110V FDA UDI
Model / Reference
9828 FDA UDI
Description
TRANSFORMER FOR LIST NO 9825 (HEADLIGHT), 110V FDA UDI

Identifiers

Catalog Number
9828 FDA UDI
Primary DI / UDI-DI
00198506073601 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Head-worn lamp

Elmed Incorporated by Elmed Incorporated — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Elmed Incorporated

Sources (1)

  • FDA UDI ee2ded4d-acbd-4cce-8634-2f504f4031f3 35 fields · synced Jun 8, 2026