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Princess

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
PRINCESS FDA UDI
Generic Name
Endoscope sheath, reusable FDA UDI
Device Name
INNER SHEATH RESECTOSCOPE 19FR color code black, SL 211 mm, round, non-rotatable, distal end beveled, compatible with outer sheath 8653.021 for Princess resectoscope 21 Fr with continuous irrigation, and telescopes Ø 2.7 mm, 12°, with Luer connection, E-Line quick connection, reusable FDA UDI
Model / Reference
8653018 FDA UDI
Description
INNER SHEATH RESECTOSCOPE 19FR color code black, SL 211 mm, round, non-rotatable, distal end beveled, compatible with outer sheath 8653.021 for Princess resectoscope 21 Fr with continuous irrigation, and telescopes Ø 2.7 mm, 12°, with Luer connection, E-Line quick connection, reusable FDA UDI

Identifiers

Catalog Number
8653.018 FDA UDI
Primary DI / UDI-DI
04055207042861 FDA UDI
FDA Product Code
FDC FDA UDI
GMDN Term
Endoscope sheath, reusable 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: Endoscope sheath, reusable

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

Similar devices

Also classified as Endoscope sheath, reusable.

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 a107b7c9-18b9-418d-83e9-e0a25c635269 36 fields · synced May 30, 2026