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Phantom Bone Collector, Single-Use, Sterile
FDA UDIClass II (US FDA UDI)
by Morpheus AG
Identity
- Trade Name
- PHANTOM BONE COLLECTOR, SINGLE-USE, STERILE FDA UDI
- Generic Name
- Orthopaedic surgery tissue debris collector, single-use FDA UDI
- Device Name
- BONE COLLECTOR, SINGLE-USE, STERILE FDA UDI
- Model / Reference
- KR-0100 FDA UDI
- Description
- BONE COLLECTOR, SINGLE-USE, STERILE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04260647240139 FDA UDI
- FDA Product Code
- BYZ FDA UDI
- GMDN Term
- Orthopaedic surgery tissue debris collector, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- 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
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Orthopaedic surgery tissue debris collector, single-use
Phantom Bone Collector, Single-Use, Sterile by Morpheus AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic surgery tissue debris collector, single-use.
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- Osteomedix, Inc. — OSTEOMEDIX, INC. · Class II
- Tobra Bone Basket — TOBRA MEDICAL, INC. · Class II
- spineX BONE DUST COLLECTOR — Oto-Med, Inc. · Class II
- OsteoPoint — Morpheus AG · Class II
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
- Morpheus AG
Sources (1)
- FDA UDI 1429bd86-fbf9-403a-81f8-998a2f45fc67 33 fields · synced Jun 8, 2026