Identity
- Trade Name
- MORCE POWER PLUS FDA UDI
- Generic Name
- Tissue morcellation system FDA UDI
- Device Name
- CUTTING TUBE Ø 20MM PACK=1 PC, WL 210mm, for use with handpiece 8307011, for fragmentation of tissue, in gynecology, reusable FDA UDI
- Model / Reference
- 8307020 FDA UDI
- Description
- CUTTING TUBE Ø 20MM PACK=1 PC, WL 210mm, for use with handpiece 8307011, for fragmentation of tissue, in gynecology, reusable FDA UDI
Identifiers
- Catalog Number
- 8307020 FDA UDI
- Primary DI / UDI-DI
- 04055207000977 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 20 Millimeter 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Richard Wolf GmbH
Sources (1)
- FDA UDI 3cecfbe9-7857-49dd-a0a9-ed06635d4ec2 37 fields · synced Jun 1, 2026