Headrest MTSILVER2A
by Medtec LLC
Part of a family of 108 devices: see the family page
Ref MTSILVER2AModel Head, Neck, and Shoulder Devices
Headrest MTSILVER2A is a device classified as Class I in the EU and Class II in the US made by Medtec LLC, registered in EUDAMED on 22 May 2026 (Basic UDI-DI 8414391OC0005R01AQ), cleared under FDA 510(k) K080072 on 4 Jun 2008 (1 earlier submission) and listed in FDA GUDID since 2 Aug 2017 (UDI-DI 00841439107683), active as of 22 Oct 2026. 2 FDA recalls are linked to it.
Active
Valid until
No date given
FDA recalls
None ongoingTrust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number8414391OC0005R01AQ 00841439107683 | Date22 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00841439107683 | Date2 Aug 2017 | StatusListed |
| United States | FDA 510(k)SESE GUDID | NumberK080072 | Date4 Jun 2008 | StatusActive |
Official records
- EUDAMED public site 8414391OC0005R01AQ
- AccessGUDID record 00841439107683
- FDA 510(k) database K080072
- FDA 510(k) database K933227
Across registries
- EUDAMED Basic UDI-DI 8414391OC0005R01AQ registered 22 May 2026 Active
- FDA 510(k) K080072 decided 4 Jun 2008 Active
- FDA GUDID UDI-DI 00841439107683 listed 2 Aug 2017 Listed
Recalls
-
- Terminated Z-2243-2020
Potential for disengagement of the Varian Style Type-S Extension during patient repositioning. The risk associated with the disengagement of the extension could be a patient fall if the patient is not supported by clinical staff.
-
- Terminated Z-0124-2010
Some of the packages contain the incorrect mask style.
Timeline
- Cleared FDA 510(k) K933227
- Cleared FDA 510(k) K080072
- Recall initiated FDA recalls Z-0124-2010
- Listed FDA GUDID 00841439107683
- Recall initiated FDA recalls Z-2243-2020
- Registered EUDAMED 8414391OC0005R01AQ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Headrest
- Generic name
- Radiological headrest
- Model / Ref / Catalog
- MTSILVER2A, Head, Neck, and Shoulder Devices
- Primary DI / UDI-DI
- 00841439107683
- Basic UDI-DI
- 8414391OC0005R01AQ
- FDA product code
- IYE
- EMDN code
- Z12011299 Patient positioning instruments – other
- GMDN term
- Radiological headrest
- Device class
- Class I EUDAMEDClass II GUDID
- Regulation number
- 892.5050
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
- Size
- Length — 11 Inch
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class I | Class II |
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