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Hcs

FDA UDI

Class I (US FDA UDI)

by Dyad Medical Sourcing, Llc

Identity

Trade Name
HCS FDA UDI
Generic Name
Hand-held examination/treatment light FDA UDI
Device Name
Examination Penlights FDA UDI
Model / Reference
HCS8015 FDA UDI
Description
Examination Penlights FDA UDI

Identifiers

Primary DI / UDI-DI
00849027004383 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

Hcs by Dyad Medical Sourcing, Llc — 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 edbaeb56-b3ea-422a-aa7a-e56031866b48 33 fields · synced May 31, 2026