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C3

FDA UDI

Class I (US FDA UDI)

by Qed, Inc.

Identity

Trade Name
C3 FDA UDI
Generic Name
Head-worn lamp FDA UDI
Device Name
Portable LED Headlight FDA UDI
Model / Reference
QED-9700 FDA UDI
Description
Portable LED Headlight FDA UDI

Identifiers

Primary DI / UDI-DI
00860013851545 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Head-worn lamp

C3 by Qed, Inc. — 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

Manufacturer
Qed, Inc.

Sources (1)

  • FDA UDI 4449d5c3-6b83-441e-9505-c02aa5f49474 34 fields · synced May 31, 2026