← Back to catalogue

KaWe

FDA UDI

Class I (US FDA UDI)

by Medical, Inc.

Identity

Trade Name
KaWe FDA UDI
Generic Name
Hand-held examination/treatment light FDA UDI
Device Name
KaWe Cliplight Diagnostic Penlight, Navy Blue FDA UDI
Model / Reference
60-640-180 FDA UDI
Description
KaWe Cliplight Diagnostic Penlight, Navy Blue FDA UDI

Identifiers

Primary DI / UDI-DI
00845821001269 FDA UDI
FDA Product Code
KYT FDA UDI
GMDN Term
Hand-held examination/treatment light FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6350 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: Hand-held examination/treatment light

KaWe by Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held examination/treatment light.

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
Medical, Inc.

Sources (1)

  • FDA UDI d1946439-cce5-48a7-852c-0f4e175c0b87 34 fields · synced Jun 8, 2026