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Emergency Stretcher

by Zhangjiagangtengda Machinery Manufacturer Co., Ltd 19 variants

Ref MLF999-E/TD01016/TD01016AModel MLF999-C1, MLF999-C2, MLF999-C3, MLF999-C, MLF999-CA, MLF999-B, MLF999-B1, MLF999-A3-1, MLF999-A3-2, MLF999-A3-3, MLF999-F1, MLF999-F2, MLF999E, TD010161, TD010163, MLF999-E1, MLF999-A, MLF999-D, TD+1

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Overview

A medical device designed for emergency situations, providing a secure and reliable way to stretch the body. This device is ideal for use in emergency response situations where timely action is crucial.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697486666STRETCHERX4 Basic UDI-DI 06974866660132UDI-DIDate13 Mar 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Emergency Stretcher
Model / Reference
MLF999-C1, MLF999-C2, MLF999-C3, MLF999-C, MLF999-CA, MLF999-B, MLF999-B1, MLF999-A3-1, MLF999-A3-2, MLF999-A3-3, MLF999-F1, MLF999-F2, MLF999E, TD010161, TD010163, MLF999-E1, MLF999-A, MLF999-D, TD+1, MLF999-E/TD01016/TD01016A
Primary DI / UDI-DI
06974866660132
Basic UDI-DI
697486666STRETCHERX4
EMDN Code
V08050103 Emergency and traumatology stretchers
Device Class
Class I
EU market of registration
Bulgaria

Manufacturer details

EUDAMED SRN
CN-MF-000013468
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

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Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No