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Tipcontrol

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
TIPCONTROL FDA UDI
Generic Name
Endoscopic electrosurgical electrode, bipolar, single-use FDA UDI
Device Name
RF INSTRUMENT BIPO Ø 2.5MM WL 350MM for endoscopic spine surgery, flexible insert, integrated connection cable WL 3m with device plug to Radioblator RF 4MHz, sterile, for single use FDA UDI
Model / Reference
4993692 FDA UDI
Description
RF INSTRUMENT BIPO Ø 2.5MM WL 350MM for endoscopic spine surgery, flexible insert, integrated connection cable WL 3m with device plug to Radioblator RF 4MHz, sterile, for single use FDA UDI

Identifiers

Catalog Number
4993692 FDA UDI
Primary DI / UDI-DI
04055207054215 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, bipolar, single-use 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

No

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

Dimensions & Sizes

Size
Outer Diameter — 2.5 Millimeter FDA UDI
Length — 350 Millimeter FDA UDI

Category: Endoscopic electrosurgical electrode, bipolar, single-use

Tipcontrol by Richard Wolf GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical electrode, bipolar, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Richard Wolf GmbH

Sources (1)

  • FDA UDI bd449b42-0426-445a-8be8-6d5d059bdd13 37 fields · synced May 30, 2026