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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 ™ OROTRACHEAL LIGHTED INTUBATION STYLET 16" (40CM) FDA UDI
Model / Reference
SLOT FDA UDI
Description
SURCH-LITE ™ OROTRACHEAL LIGHTED INTUBATION STYLET 16" (40CM) FDA UDI

Identifiers

Catalog Number
SLOT FDA UDI
Primary DI / UDI-DI
00607151063399 FDA UDI
FDA Product Code
BSR FDA UDI
GMDN Term
Hand-held examination/treatment light FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5790 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

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

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Manufacturer

Manufacturer
Bovie Medical Corporation

Sources (1)

  • FDA UDI 44ca0216-a9dd-4ced-8d38-05f8fac1d77a 35 fields · synced May 30, 2026