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Bovie

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Bovie FDA UDI
Generic Name
Electrocautery system generator, battery-powered FDA UDI
Device Name
Cautery High-Temp 5" Loop Tip (10/bx) FDA UDI
Model / Reference
AA09 FDA UDI
Description
Cautery High-Temp 5" Loop Tip (10/bx) FDA UDI

Identifiers

Primary DI / UDI-DI
10887482177324 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

Yes

FDA UDI

Dimensions & Sizes

Size
Shaft Length — 5 Inch FDA UDI

Category: Electrocautery system generator, battery-powered

Bovie by Symmetry Surgical Inc. — 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
Symmetry Surgical Inc.

Sources (1)

  • FDA UDI ad175d8b-54fd-4ea3-82d4-68ac0d806da5 36 fields · synced May 30, 2026