Identity
- Trade Name
- Target Tracking FDA UDI
- Generic Name
- Biomechanical function analysis/rehabilitation software FDA UDI
- Model / Reference
- V2.3.4 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03760310780104 FDA UDI
- FDA Product Code
- ISD FDA UDI
- GMDN Term
- Biomechanical function analysis/rehabilitation software FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5360 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Biomechanical function analysis/rehabilitation software
Target Tracking by Virtualis — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- mymobility® Platform — Zimmer Us, Inc. · Class I
- BioStamp nPoint™ — Medidata Solutions, Inc. · Class II
- NeckCare Exercises — NeckCare Holding ehf · Class II
- mymobility® Platform — Zimmer Us, Inc. · Class I
- mymobility® Platform — Zimmer Us, Inc. · 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
- Virtualis
Sources (1)
- FDA UDI da30379b-1f11-461e-951b-1320b1e08852 32 fields · synced May 30, 2026