Identity
- Trade Name
- VIPER FDA UDI
- Generic Name
- Bone-screw internal spinal fixation system, non-sterile FDA UDI
- Device Name
- VIPER F2 FACET FIXATION SYSTEM SCREW 6 x 20mm FDA UDI
- Model / Reference
- 175710620 FDA UDI
- Description
- VIPER F2 FACET FIXATION SYSTEM SCREW 6 x 20mm FDA UDI
Identifiers
- Catalog Number
- 175710620 FDA UDI
- Primary DI / UDI-DI
- 10705034034874 FDA UDI
- 510(k) Number
- K101762 FDA UDI
- FDA Product Code
- MRW FDA UDI
- GMDN Term
- Bone-screw internal spinal fixation system, non-sterile FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Viper by Medos International Sàrl — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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 U | Pending data |
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Manufacturer
- Manufacturer
- Medos International Sàrl
Sources (1)
- FDA UDI 4ba4a287-31ed-4fc9-93b1-1458bedaa186 37 fields · synced May 31, 2026