← Back to catalogue

Accu-temp

FDA UDI

Class II (US FDA UDI)

by Beaver-Visitec International, Inc.

Identity

Trade Name
Accu-temp FDA UDI
Generic Name
Electrocautery system generator, battery-powered FDA UDI
Device Name
ACCU-TEMP® CAUTERY VARIABLE LOW TEMP 0.5 FINE TIP 10/BX FDA UDI
Model / Reference
8440000 FDA UDI
Description
ACCU-TEMP® CAUTERY VARIABLE LOW TEMP 0.5 FINE TIP 10/BX FDA UDI

Identifiers

Catalog Number
8440000 FDA UDI
Primary DI / UDI-DI
30886158010235 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

Yes

FDA UDI

Category: Electrocautery system generator, battery-powered

Accu-temp by Beaver-Visitec International, 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

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

Manufacturer

Manufacturer
Beaver-Visitec International, Inc.

Sources (1)

  • FDA UDI 357c2ecb-1e97-45e9-8a7c-32b113920e5c 34 fields · synced Jun 1, 2026