Identity
- Trade Name
- RIWOLITH FDA UDI
- Generic Name
- Electrohydraulic lithotripsy system FDA UDI
- Device Name
- PROBE 3.3FR WL 1050MM PACK=3 PCS, sterile, for single use FDA UDI
- Model / Reference
- 2280433 FDA UDI
- Description
- PROBE 3.3FR WL 1050MM PACK=3 PCS, sterile, for single use FDA UDI
Identifiers
- Catalog Number
- 2280.433 FDA UDI
- Primary DI / UDI-DI
- 04055207038147 FDA UDI
- FDA Product Code
- FFK FDA UDI
- GMDN Term
- Electrohydraulic lithotripsy system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.4480 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 1050 Millimeter FDA UDIOuter Diameter — 1.1 Millimeter FDA UDI
Riwolith 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 ed8e1259-0f4c-4bd2-b822-d28e12ba7d28 38 fields · synced Jun 1, 2026