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Bovie

FDA UDI

Class II (US FDA UDI)

by Bovie Medical Corporation

Identity

Trade Name
Bovie FDA UDI
Generic Name
Electrocautery system generator, battery-powered FDA UDI
Device Name
CAUTERY HIGH TEMP FINE TIP 2'' EXTENDED SHAFT FDA UDI
Model / Reference
AA17 FDA UDI
Description
CAUTERY HIGH TEMP FINE TIP 2'' EXTENDED SHAFT FDA UDI

Identifiers

Catalog Number
AA17 FDA UDI
Primary DI / UDI-DI
00607151011192 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrocautery system generator, battery-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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: Electrocautery system generator, battery-powered

Bovie by Bovie Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocautery system generator, battery-powered.

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 8e8195d3-8a0e-40fd-9333-2716830a39ad 35 fields · synced Jun 8, 2026