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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, bipolar, single-use FDA UDI
Device Name
CUTTING ELECTRODE BIPO 27FR for hysteroscopy, for sheaths with chip suction, 27, Fr, loop: round, wire Ø 0.25mm, PACK=3 PCS, for use in combination with the Resection Master resectoscope, sterile, for single use FDA UDI
Model / Reference
46591613 FDA UDI
Description
CUTTING ELECTRODE BIPO 27FR for hysteroscopy, for sheaths with chip suction, 27, Fr, loop: round, wire Ø 0.25mm, PACK=3 PCS, for use in combination with the Resection Master resectoscope, sterile, for single use FDA UDI

Identifiers

Catalog Number
4659.1613 FDA UDI
Primary DI / UDI-DI
04055207048986 FDA UDI
FDA Product Code
FAS FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, bipolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4300 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 — 9 Millimeter FDA UDI

Category: Endoscopic electrosurgical electrode, bipolar, single-use

Resection Master 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 f926c123-48f1-41e0-b7ba-4253d7823dad 37 fields · synced Jun 1, 2026