Identity
- Trade Name
- MORCE POWER PLUS FDA UDI
- Generic Name
- Tissue morcellation system FDA UDI
- Device Name
- MOTOR CONTROL UNIT 2307 for Gynecology, for connection of handpiece 80951.0002, connection possible for a handpiece and a footswitch, LED-Display, U: 230 VAC, 50/60 Hz, Dim. (wxhxd): 120x115x180mm FDA UDI
- Model / Reference
- 2307101 FDA UDI
- Description
- MOTOR CONTROL UNIT 2307 for Gynecology, for connection of handpiece 80951.0002, connection possible for a handpiece and a footswitch, LED-Display, U: 230 VAC, 50/60 Hz, Dim. (wxhxd): 120x115x180mm FDA UDI
Identifiers
- Catalog Number
- 2307101 FDA UDI
- Primary DI / UDI-DI
- 04055207000502 FDA UDI
- FDA Product Code
- HET FDA UDI
- GMDN Term
- Tissue morcellation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.1720 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
Morce Power Plus 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 67d9635c-73e2-426b-b76d-6af31bbd4bb8 36 fields · synced May 31, 2026