Identity
- Trade Name
- POWER DRIVE ART1 FDA UDI
- Generic Name
- Foot-switch, electrical FDA UDI
- Device Name
- FOOTSWITCH 2 PEDALS for Power Drive ART1 Motor Control Unit FDA UDI
- Model / Reference
- 2304901 FDA UDI
- Description
- FOOTSWITCH 2 PEDALS for Power Drive ART1 Motor Control Unit FDA UDI
Identifiers
- Catalog Number
- 2304.901 FDA UDI
- Primary DI / UDI-DI
- 04055207056677 FDA UDI
- FDA Product Code
- HWE FDA UDI
- GMDN Term
- Foot-switch, electrical FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Power Drive Art1 by Richard Wolf GmbH — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Richard Wolf GmbH
Sources (1)
- FDA UDI c87c6ef1-e4ff-4cdf-aa68-735ae415faba 36 fields · synced May 30, 2026