Identity
- Trade Name
- Pure Vue FDA UDI
- Generic Name
- Software upgrade/unlocking key FDA UDI
- Device Name
- Pure Vue Software expansion FDA UDI
- Model / Reference
- 242329 FDA UDI
- Description
- Pure Vue Software expansion FDA UDI
Identifiers
- Catalog Number
- 242329 FDA UDI
- Primary DI / UDI-DI
- 10886705032204 FDA UDI
- FDA Product Code
- FCW FDA UDIGCJ FDA UDI
- GMDN Term
- Software upgrade/unlocking key FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Software upgrade/unlocking key
Pure Vue by Medos International Sàrl — 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
- Medos International Sàrl
Sources (1)
- FDA UDI a1ec76f4-2d28-4c98-beda-285170f7c2df 36 fields · synced Jun 8, 2026