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Adlite™ Plus

FDA UDI

Class I (US FDA UDI)

by American Diagnostic Corporation

Identity

Trade Name
Adlite™ Plus FDA UDI
Generic Name
Hand-held examination/treatment light FDA UDI
Device Name
ADLITE Plus Disp Penlight,22/cyl, Teal, Purple, Black FDA UDI
Model / Reference
358TVB FDA UDI
Description
ADLITE Plus Disp Penlight,22/cyl, Teal, Purple, Black FDA UDI

Identifiers

Catalog Number
358TVB FDA UDI
Primary DI / UDI-DI
00634782040321 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

Yes

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

No

FDA UDI

Category: Hand-held examination/treatment light

Adlite™ Plus by American Diagnostic Corporation — 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

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Manufacturer

Sources (1)

  • FDA UDI 8bef3319-9b99-4e24-9402-2b70fceb52f3 35 fields · synced Jun 8, 2026