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Headrest MTLTBPIAT01

by Medtec LLC

Ref MTLTBPIAT01Model Head, Neck, and Shoulder Devices

Headrest MTLTBPIAT01 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) K933227 on 18 Jul 1994 and listed in FDA GUDID since 2 Aug 2017 (UDI-DI 00841439106532), active as of 22 Oct 2026. 2 FDA recalls are linked to it.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None ongoing

2 closed

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K933227

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number8414391OC0005R01AQ Basic UDI-DI 00841439106532UDI-DIDate22 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00841439106532 UDI-DI Date2 Aug 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK933227 Date18 Jul 1994DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 8414391OC0005R01AQ registered 22 May 2026 Active
  • FDA 510(k) K933227 decided 18 Jul 1994 Active
  • FDA GUDID UDI-DI 00841439106532 listed 2 Aug 2017 Listed

Recalls

2 recalls · FDA

    • Terminated Z-2243-2020 FDA Class II initiated 12 May 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 FDA Unclassified (pre-2012) initiated 31 Aug 2009

    Some of the packages contain the incorrect mask style.

Timeline

5 dated events

  1. Cleared FDA 510(k) K933227
  2. Recall initiated FDA recalls Z-0124-2010
  3. Listed FDA GUDID 00841439106532
  4. Recall initiated FDA recalls Z-2243-2020
  5. Registered EUDAMED 8414391OC0005R01AQ

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Headrest
Generic name
Radiological headrest
Model / Ref / Catalog
MTLTBPIAT01, Head, Neck, and Shoulder Devices
Primary DI / UDI-DI
00841439106532
Basic UDI-DI
8414391OC0005R01AQ
510(k) Number
FDA product code
IYE
EMDN code
Z12011299 Patient positioning instruments – other
GMDN term
Radiological headrest
Device class
Class I EUDAMED
Class II GUDID
Regulation number
892.5050
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Size
Width — 22 Centimeter
Length — 23 Centimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Radiological headrest

Cleared under the same submission (K933227)

and 8 more cleared under K933227

Similar devices in this category

Other devices filed under PATIENT POSITIONING INSTRUMENTS – OTHER.

Other devices from Medtec LLC

See all devices from Medtec LLC →

Properties

  • Reusable
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)