← Back to catalogue

Bovie

FDA UDI

Class I (US FDA UDI)

by Bovie Medical Corporation

Identity

Trade Name
Bovie FDA UDI
Generic Name
Hand-held examination/treatment light FDA UDI
Device Name
SURCH-LITE ™ MEDICAL LIGHT NON-STERILE 5'' (12.5cm) FDA UDI
Model / Reference
NS05 FDA UDI
Description
SURCH-LITE ™ MEDICAL LIGHT NON-STERILE 5'' (12.5cm) FDA UDI

Identifiers

Catalog Number
NS05 FDA UDI
Primary DI / UDI-DI
00607151086053 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

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hand-held examination/treatment light

Bovie by Bovie Medical 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Bovie Medical Corporation

Sources (1)

  • FDA UDI 2fa4759e-2af7-45e0-b2b8-6f32d6c1be6b 35 fields · synced Jun 8, 2026