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Emergency bed

by Suzhou Ireland Medical Equipment Co., Ltd. 19 variants

Ref DW-ET03, DW-ET05, DW-ET16, DW-ST017, DW-ET02, DW-ET10, DW-ST016, DW-ET11, DW-ET18, DW-ET28, DW-ET14, DW-ET27, DW-ET19, DW-ST018, DW-ST019, DW-ET29, DW-ET26, DW-ET01, DW-ET23, DW-ET09, DW-ET21, DW-ST010, DW-ET20, DW-SS007, DW-ET07, DW-D107, DW-ST020, DW-ET24, DW-ST012, DW-ET06A, DW-ET17, DW-ET08

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697772854DWEBV8 Basic UDI-DI Date20 Aug 2024RegisteredStatusActive

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  • Withdrawn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

Model / Reference
DW-ET03, DW-ET05, DW-ET16, DW-ST017, DW-ET02, DW-ET10, DW-ST016, DW-ET11, DW-ET18, DW-ET28, DW-ET14, DW-ET27, DW-ET19, DW-ST018, DW-ST019, DW-ET29, DW-ET26, DW-ET01, DW-ET23, DW-ET09, DW-ET21, DW-ST010, DW-ET20, DW-SS007, DW-ET07, DW-D107, DW-ST020, DW-ET24, DW-ST012, DW-ET06A, DW-ET17, DW-ET08
Primary DI / UDI-DI
06977728542096, 06977728542119, 06977728542232, 06977728542485, 06977728542089, 06977728542171, 06977728542478, 06977728542188, 06977728542256, 06977728542355, 06977728542218, 06977728542348, 06977728542263, 06977728542492, 06977728542508, 06977728542362, 06977728542331, 06977728542072, 06977728542300, 06977728542164, 06977728542287, 06977728542416, 06977728542270, 06977728542539, 06977728542140, 06977728542560, 06977728542515, 06977728542317, 06977728542430, 06977728542133, 06977728542249, 06977728542157
Basic UDI-DI
697772854DWEBV8
Direct Marketing DI
06977728542096
06977728542119
06977728542232
06977728542485
06977728542089
06977728542171
06977728542478
06977728542188
06977728542256
06977728542355
06977728542218
06977728542348
06977728542263
06977728542492
06977728542508
06977728542362
06977728542331
06977728542072
06977728542300
06977728542164
06977728542287
06977728542416
06977728542270
06977728542539
06977728542140
06977728542560
06977728542515
06977728542317
06977728542430
06977728542133
06977728542249
06977728542157
EMDN Code
V08050103 Emergency and traumatology stretchers
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000043757
Authorised representative
MedPath GmbH DE-AR-000000087

Other devices from Suzhou Ireland Medical Equipment Co., Ltd.

See all devices from Suzhou Ireland Medical Equipment Co., Ltd. →

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