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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 TEMPERATURE ELONGATED TIP FDA UDI
Model / Reference
AA21 FDA UDI
Description
CAUTERY HIGH TEMPERATURE ELONGATED TIP FDA UDI

Identifiers

Catalog Number
AA21 FDA UDI
Primary DI / UDI-DI
00607151011215 FDA UDI
FDA Product Code
HQP FDA UDI
GMDN Term
Electrocautery system generator, battery-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4115 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 4b070a4d-a8e1-4961-8544-7b34ea898e13 35 fields · synced Jun 8, 2026