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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
Rigid endoscope obturator FDA UDI
Device Name
OBTURATOR RESECTOSCOPE color code yellow, for WL 202mm, round, distal tip dull, compatible with outer sheath 8659071 for Resection Master Resectoscope 27Fr with integrated chip suction, reusable FDA UDI
Model / Reference
8659175 FDA UDI
Description
OBTURATOR RESECTOSCOPE color code yellow, for WL 202mm, round, distal tip dull, compatible with outer sheath 8659071 for Resection Master Resectoscope 27Fr with integrated chip suction, reusable FDA UDI

Identifiers

Catalog Number
8659.175 FDA UDI
Primary DI / UDI-DI
04055207019108 FDA UDI
FDA Product Code
FJL FDA UDI
GMDN Term
Rigid endoscope obturator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
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

Category: Rigid endoscope obturator

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

Similar devices

Also classified as Rigid endoscope obturator.

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 1d45231b-effa-46ac-82c2-4e2883aad110 35 fields · synced May 30, 2026