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ABC® Bend-A-Beam®

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
ABC® Bend-A-Beam® FDA UDI
Generic Name
Inert gas-enhanced open-surgery electrosurgical handpiece/electrode FDA UDI
Device Name
ABC® Bend-A-Beam® Handpiece Handcontrol Malleable Handpiece, 3" (7.6 cm) FDA UDI
Model / Reference
134003 FDA UDI
Description
ABC® Bend-A-Beam® Handpiece Handcontrol Malleable Handpiece, 3" (7.6 cm) FDA UDI

Identifiers

Catalog Number
134003 FDA UDI
Primary DI / UDI-DI
30653405002745 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Inert gas-enhanced open-surgery electrosurgical handpiece/electrode 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

Yes

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: Inert gas-enhanced open-surgery electrosurgical handpiece/electrode

ABC® Bend-A-Beam® by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inert gas-enhanced open-surgery electrosurgical handpiece/electrode.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 78ceba3e-5f36-4e39-b1e7-62d5e5989dc6 36 fields · synced Jun 1, 2026