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Phantom Multi-Bite Kerrison Rongeur
FDA UDIClass II (US FDA UDI)
by Morpheus AG
Identity
- Trade Name
- PHANTOM MULTI-BITE KERRISON RONGEUR FDA UDI
- Generic Name
- Orthopaedic joint/limb rongeur FDA UDI
- Device Name
- MULTI-BITE KERRISON RONGEUR 2 MM BITE SIZE, 14 MM OPEN, 200 MM (7.9") LENGTH, SINGLE-USE, STERILE FDA UDI
- Model / Reference
- KR-2002 FDA UDI
- Description
- MULTI-BITE KERRISON RONGEUR 2 MM BITE SIZE, 14 MM OPEN, 200 MM (7.9") LENGTH, SINGLE-USE, STERILE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04260647240061 FDA UDI
- FDA Product Code
- HAE FDA UDI
- GMDN Term
- Orthopaedic joint/limb rongeur FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4840 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
No
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 joint/limb rongeur
Phantom Multi-Bite Kerrison Rongeur by Morpheus AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Orthopaedic joint/limb rongeur.
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- Hayden Medical — Hayden Medical Inc · Class I
- MICRO FRIEDMAN RONGEUR — SONTEC INSTRUMENTS, INC. · Class I
- Sklar® — Sklar Corporation · Class I
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 18a553cf-4b75-4bbd-8335-f25548d4d3e4 33 fields · synced May 30, 2026