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Princess

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
PRINCESS FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI
Device Name
ROLLER ELECTRODE MONO 21/24.5FR for hysteroscopy, for continuous irrigation sheaths, 21/ 24.5, Fr, electrode shape: roller, fork color red, stem color blue, PACK=1 PC, for use in combination with the Princess resectoscope, unsterile, reusable FDA UDI
Model / Reference
865302 FDA UDI
Description
ROLLER ELECTRODE MONO 21/24.5FR for hysteroscopy, for continuous irrigation sheaths, 21/ 24.5, Fr, electrode shape: roller, fork color red, stem color blue, PACK=1 PC, for use in combination with the Princess resectoscope, unsterile, reusable FDA UDI

Identifiers

Catalog Number
8653.02 FDA UDI
Primary DI / UDI-DI
04055207040744 FDA UDI
FDA Product Code
FDC FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Princess 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

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Manufacturer

Manufacturer
Richard Wolf GmbH

Sources (1)

  • FDA UDI f87a83b1-2ced-49a5-9f6c-bad794858768 36 fields · synced Jun 8, 2026