Identity
- Trade Name
- PRINCESS FDA UDI
- Generic Name
- Rigid endoscope obturator FDA UDI
- Device Name
- VIEWING OBTURATOR RESECTOSCOPE 19FR color code black, for WL 230 mm, hollow and atraumatic distal tip, compatible with inner sheath 8653.018 and 8653019 for Princess resectoscope 21 Fr with continuous irrigation, and telescopes Ø 2.7 mm, 12°, automatic click connection, reusable FDA UDI
- Model / Reference
- 865319 FDA UDI
- Description
- VIEWING OBTURATOR RESECTOSCOPE 19FR color code black, for WL 230 mm, hollow and atraumatic distal tip, compatible with inner sheath 8653.018 and 8653019 for Princess resectoscope 21 Fr with continuous irrigation, and telescopes Ø 2.7 mm, 12°, automatic click connection, reusable FDA UDI
Identifiers
- Catalog Number
- 865319 FDA UDI
- Primary DI / UDI-DI
- 04055207010839 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
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 6.33333333333 Millimeter 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.
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- Trabecular Metal® — Zimmer, Inc. · Class I
- Obturator — SOPRO-COMEG GmbH · Class II
- Obturator — SOPRO-COMEG GmbH · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Richard Wolf GmbH
Sources (1)
- FDA UDI 755fb7b2-c25b-4c9b-9b0e-e158cfb61a78 37 fields · synced May 30, 2026