Viper System
EUDAMEDFDA UDIClass IIb (EU MDR)
Identity
- Trade Name
- VIPER SYSTEM EUDAMEDEXPEDIUM FDA UDI
- Generic Name
- Spinal bone screw, non-bioabsorbable FDA UDI
- Device Name
- Viper Spine System Bone Screws Cannulated Polyaxial Screw, Cannulated Monoaxial Screw, Cannulated Uniplanar Screw, Cannulated Extended Tab Polyaxial Screw, Polyaxial Wide Lag Screw, Polyaxial Fully Threaded Screw, X-TAB Polyaxial Screw, CFX X-TAB Polyaxi EUDAMEDVIPER SYSTEM POLYAXIAL FULLY THREADED SCREW 5.5 10 x 70mm FDA UDI
- Model / Reference
- VIPER Spine System Bone Screws EUDAMED179706070 EUDAMEDFDA UDI
- Description
- VIPER SYSTEM POLYAXIAL FULLY THREADED SCREW 5.5 10 x 70mm FDA UDI
Identifiers
- Catalog Number
- 179706070 FDA UDI
- Primary DI / UDI-DI
- 10705034266305 EUDAMEDFDA UDI
- Basic UDI-DI
- 0705034a002065S EUDAMED
- 510(k) Number
- K111571 FDA UDI
- FDA Product Code
- MNI FDA UDINKB FDA UDIKWP FDA UDIMNH FDA UDI
- EMDN Code
- P09070302 THORACOLUMBOSACRAL FIXATION SYSTEMS EUDAMED
- GMDN Term
- Spinal bone screw, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 888.3070 FDA UDI888.3050 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
Yes
Implantable
Yes
Reusable
No
Contains Latex
No
Reprocessed
No
Sutures
Yes
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
No
Category: Spinal bone screw, non-bioabsorbable
Viper System by Medos International Sarl — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Spinal bone screw, non-bioabsorbable.
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- AccelFix Spinal Fixation System (Sterile) — L&K Biomed · Class IIb
- Proficient™ Posterior Cervical Spine System — Spine Wave, Inc. · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0705034a002065S | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- Medos International SARL
- EUDAMED SRN
- CH-MF-000014268
- Authorised Representative
- DePuy Ireland UC IE-AR-000009328
Sources (2)
- EUDAMED d5eaff0d-3d1c-4f25-badf-4cedd8e0044f 61 fields · synced May 30, 2026
- FDA UDI e3c88ec8-e0aa-4d2c-acac-bcd4c83a38c7 36 fields · synced May 30, 2026