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Rebreathing bag

by Hsiner Co., Ltd. 5 variants

Ref 70502

Rebreathing bag (70502) is a Class IIa device made by Hsiner Co., Ltd., registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI B-04712688057868), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04712688057868 Basic UDI-DI 04712688057868UDI-DIDate4 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Rebreathing bag
Model / reference
70502
Primary DI / UDI-DI
04712688057868
Basic UDI-DI
B-04712688057868
EMDN code
R03020101 Anaesthesia balloons
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
TW-MF-000007258
Authorised representative
mdi Europa GmbH DE-AR-000006218

Similar devices in this category

Other devices filed under ANAESTHESIA BALLOONS.

Other devices from Hsiner Co., Ltd.

See all devices from Hsiner Co., Ltd. →

Properties

Other properties (12, all answered No)