Identity
- Trade Name
- MR-RT FDA UDI
- Generic Name
- Radiation therapy treatment planning positioning kit FDA UDI
- Device Name
- MR-RT is an add-on to the existing Ingenia 1.5T and 3.0T MR systems that makes the system suitable for MR imaging for radiation therapy planning purposes. FDA UDI
- Model / Reference
- RT CouchTop XD FDA UDI
- Description
- MR-RT is an add-on to the existing Ingenia 1.5T and 3.0T MR systems that makes the system suitable for MR imaging for radiation therapy planning purposes. FDA UDI
Identifiers
- Catalog Number
- 781439 FDA UDI
- Primary DI / UDI-DI
- 00884838103528 FDA UDI
- FDA Product Code
- LNH FDA UDI
- GMDN Term
- Radiation therapy treatment planning positioning kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1000 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Mr-Rt by Philips Oy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Philips Oy
Sources (1)
- FDA UDI c31a57b2-0c2f-4489-adab-b6ecf1e2961c 36 fields · synced Jun 8, 2026