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Princess

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
PRINCESS FDA UDI
Generic Name
Rigid endoscope obturator FDA UDI
Device Name
OBTURATOR RESECTOSCOPE 19FR color code black, for WL 230 mm, distal tip dull, compatible with inner sheath 8653.018 and 8653019 for Princess resectoscope 21 Fr with continuous irrigation, reusable FDA UDI
Model / Reference
865318 FDA UDI
Description
OBTURATOR RESECTOSCOPE 19FR color code black, for WL 230 mm, distal tip dull, compatible with inner sheath 8653.018 and 8653019 for Princess resectoscope 21 Fr with continuous irrigation, reusable FDA UDI

Identifiers

Catalog Number
8653.18 FDA UDI
Primary DI / UDI-DI
04055207040751 FDA UDI
FDA Product Code
FDC 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

Princess 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 4317fee8-002c-4b4e-86d3-76456157f41e 36 fields · synced May 30, 2026