Identity
- Trade Name
- ACTEON FDA UDI
- Generic Name
- Diagnostic-imaging multiformat camera FDA UDI
- Device Name
- "The DOCK MU_USB2 module are built-in docking stations for SOPRO 617, SOPRO 717 First, SOPROCARE and SOPROLIFE cameras. This product is designed for dental applications and is not intended for diagnosis" FDA UDI
- Model / Reference
- DOCK MU USB2 FUSIBLE ADEC 7M S FDA UDI
- Description
- "The DOCK MU_USB2 module are built-in docking stations for SOPRO 617, SOPRO 717 First, SOPROCARE and SOPROLIFE cameras. This product is designed for dental applications and is not intended for diagnosis" FDA UDI
Identifiers
- Catalog Number
- S_717_1061 FDA UDI
- Primary DI / UDI-DI
- M430S71710611 FDA UDI
- FDA Product Code
- NYH FDA UDI
- GMDN Term
- Diagnostic-imaging multiformat camera FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.1740 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Diagnostic-imaging multiformat camera
Acteon by Sopro — 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
- Sopro
Sources (1)
- FDA UDI adb55310-e594-498f-9489-d20348a4e537 35 fields · synced May 31, 2026