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Dynamik Intervertebral Body Fusion Device
FDA UDIClass II (US FDA UDI)
by Spineart
Identity
- Trade Name
- Dynamik Intervertebral Body Fusion Device FDA UDI
- Generic Name
- Orthopaedic graft inserter, reusable FDA UDI
- Device Name
- GRAFT FUNNEL PLUNGER 5MM FDA UDI
- Model / Reference
- SPE-US 00 17-N FDA UDI
- Description
- GRAFT FUNNEL PLUNGER 5MM FDA UDI
Identifiers
- Catalog Number
- SPE-US 00 17-N FDA UDI
- Primary DI / UDI-DI
- 07640178985650 FDA UDI
- FDA Product Code
- MAX FDA UDI
- GMDN Term
- Orthopaedic graft inserter, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3080 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
Yes
FDA UDI
Category: Orthopaedic graft inserter, reusable
Dynamik Intervertebral Body Fusion Device by Spineart — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Spineart
Sources (1)
- FDA UDI 84014c3d-52ca-43ee-909d-012f4e8a1063 34 fields · synced May 31, 2026