← Back to catalogue

Resection Master

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
RESECTION MASTER FDA UDI
Generic Name
Endoscopic electrosurgical electrode, monopolar, reusable FDA UDI
Device Name
HOOK ELECTRODE MONO/BIPO 27FR for hysteroscopy, for sheaths with chip suction, 27, Fr, electrode shape: hook, PACK=1 PC, for use in combination with the Resection Master resectoscope, unsterile, reusable FDA UDI
Model / Reference
8659163 FDA UDI
Description
HOOK ELECTRODE MONO/BIPO 27FR for hysteroscopy, for sheaths with chip suction, 27, Fr, electrode shape: hook, PACK=1 PC, for use in combination with the Resection Master resectoscope, unsterile, reusable FDA UDI

Identifiers

Catalog Number
8659163 FDA UDI
Primary DI / UDI-DI
04055207019092 FDA UDI
FDA Product Code
FAS FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, monopolar, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4300 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 9 Millimeter FDA UDI

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

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
Richard Wolf GmbH

Sources (1)

  • FDA UDI a4f6043e-70b9-45bc-b703-3be3d8c4f446 37 fields · synced Jun 8, 2026