Identity
- Trade Name
- Connexion FDA UDI
- Generic Name
- Accelerator system table, non-powered FDA UDI
- Device Name
- The Connexion™ modular couchtop consists of a Base Board that attaches to the Precise Table and several modules which can be attached (and detached) to the Base Board. Each of the different modules is designed to fulfill specific treatment scenarios. FDA UDI
- Model / Reference
- P10105-200 FDA UDI
- Description
- The Connexion™ modular couchtop consists of a Base Board that attaches to the Precise Table and several modules which can be attached (and detached) to the Base Board. Each of the different modules is designed to fulfill specific treatment scenarios. FDA UDI
Identifiers
- Catalog Number
- P10105-200 FDA UDI
- Primary DI / UDI-DI
- 04056719001186 FDA UDI
- FDA Product Code
- IXQ FDA UDI
- GMDN Term
- Accelerator system table, non-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1980 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Accelerator system table, non-powered
Connexion by 3C-Medical Intelligence GmbH — 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
- 3C-Medical Intelligence GmbH
Sources (1)
- FDA UDI 7ca3bac7-40ba-493c-95f9-2cba82919957 34 fields · synced Jun 8, 2026