Identity
- Trade Name
- Protura FDA UDI
- Generic Name
- Indexed-immobilization patient positioning system FDA UDI
- Device Name
- Protura Robotic Couch System Version 1.4.0 FDA UDI
- Model / Reference
- MT6XSM1.4.0 FDA UDI
- Description
- Protura Robotic Couch System Version 1.4.0 FDA UDI
Identifiers
- Catalog Number
- MT6XSM1.4.0 FDA UDI
- Primary DI / UDI-DI
- 00841439102855 FDA UDI
- 510(k) Number
- K132084 FDA UDI
- FDA Product Code
- JAI FDA UDI
- GMDN Term
- Indexed-immobilization patient positioning system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.5770 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 11 Inch FDA UDIWidth — 8.5 Inch FDA UDI
Protura by Medtec LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K132084 also covers:
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
- Medtec LLC
Sources (1)
- FDA UDI a6fb9267-bdb9-412e-bb10-dfbcf307cc79 38 fields · synced Jun 8, 2026