Identity
- Trade Name
- RESECTION MASTER FDA UDI
- Generic Name
- Resectoscope FDA UDI
- Device Name
- WORKING ELEMENT PASSIVE MONO/BIPO compatible Resection Master resectoscope 27Fr with integrated chip suction, and telescopes Ø 3.3mm, bayonet-cap, reusable FDA UDI
- Model / Reference
- 86592351 FDA UDI
- Description
- WORKING ELEMENT PASSIVE MONO/BIPO compatible Resection Master resectoscope 27Fr with integrated chip suction, and telescopes Ø 3.3mm, bayonet-cap, reusable FDA UDI
Identifiers
- Catalog Number
- 86592351 FDA UDI
- Primary DI / UDI-DI
- 04055207028117 FDA UDI
- FDA Product Code
- FDC FDA UDI
- GMDN Term
- Resectoscope 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
Moist Heat or Steam Sterilization FDA UDI
Resection Master 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
| 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 3bf08233-7ea3-4aa2-bbf8-7f898bad4f38 36 fields · synced May 31, 2026