← Back to catalogue
SRS MR Adapter
FDA UDIEUDAMEDClass II (US FDA UDI)
Ref RT-4600-03-MRIModel Head and Neck
by Qfix
Identity
- Trade Name
- SRS MR Adapter FDA UDI
- Generic Name
- Patient positioner base plate FDA UDI
- Device Name
- SRS MR Adapter for Portrait™ and S-Type Devices FDA UDI
- Model / Reference
- RT-4600-03-MRI EUDAMEDFDA UDIHead and Neck EUDAMED
- Description
- SRS MR Adapter for Portrait™ and S-Type Devices FDA UDI
Identifiers
- Catalog Number
- RT-4600-03-MRI FDA UDI
- Primary DI / UDI-DI
- 10841962110775 EUDAMEDFDA UDI
- Basic UDI-DI
- 8419621HEADNECKX4 EUDAMED
- FDA Product Code
- IYE FDA UDILNH FDA UDIOUO FDA UDIKPS FDA UDIJAK FDA UDIJAI FDA UDILHN FDA UDI
- EMDN Code
- Z12011299 PATIENT POSITIONING INSTRUMENTS – OTHER EUDAMED
- GMDN Term
- Patient positioner base plate FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 892.5050 FDA UDI892.1000 FDA UDI892.1200 FDA UDI892.1750 FDA UDI892.5770 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
MR Safe FDA UDI
Category: Patient positioner base plate
SRS MR Adapter by Qfix — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Patient positioner base plate.
- Meicen — Guangdong Meicen Medical Equipment Co., Ltd. · Class I
- Type-S™ Variable Axis Baseplate — Medtec LLC · Class II
- Posifix® -2 Baseplate — Medtec LLC · Class II
- MR Posi-S™ Adapter — Medtec LLC · Class II
- Uni-frame® Baseplate — Medtec LLC · Class II
- Prone Head Holder — Medtec LLC · Class I
- Arthrex TRIMANO quick adapter — Maquet, Inc. · Class I
- Uni-frame® Baseplate — Medtec LLC · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Qfix
Sources (2)
- FDA UDI 307b8459-cdf8-42eb-9086-64a84ea2456e 35 fields · synced Jun 19, 2026
- EUDAMED a36804bd-9e1a-4af5-a5bf-117423123cbf 61 fields · synced Jun 14, 2026