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Nurse-Mate®

FDA UDI

Class I (US FDA UDI)

by Beaver-Visitec International, Inc.

Identity

Trade Name
Nurse-Mate® FDA UDI
Generic Name
Hand-held examination/treatment light FDA UDI
Device Name
Six-Pack Diagnostic Penlights FDA UDI
Model / Reference
8310080 FDA UDI
Description
Six-Pack Diagnostic Penlights FDA UDI

Identifiers

Catalog Number
8310080 FDA UDI
Primary DI / UDI-DI
30886158010150 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hand-held examination/treatment light

Nurse-Mate® by Beaver-Visitec International, 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

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Manufacturer

Manufacturer
Beaver-Visitec International, Inc.

Sources (1)

  • FDA UDI 7a99c7e3-137c-4cb2-b1d9-2b2ea28a0b4f 35 fields · synced Jun 8, 2026