Ceren

by Ceren Üreti̇m Plasti̇k Ürünleri̇ Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇ 6 variants

Ref ALS 2030 2070Model REUSABLE ARTIFICIAL RESPIRATOR - ADULT

Active European Union

CE MDD

Valid until

Not listed

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

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

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-08681227070643 Basic UDI-DI 08681227070643UDI-DI	Date14 Oct 2024Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name: Reusable Artificial Respirator
Model / Reference: REUSABLE ARTIFICIAL RESPIRATOR - ADULT, ALS 2030 2070

Primary DI / UDI-DI: 08681227070643
Basic UDI-DI: B-08681227070643
EMDN Code: R03020201 Manually operated pulmonary resuscitators

Device Class: Class IIa
EU market of registration: Türkiye

Manufacturer details

EUDAMED SRN: TR-MF-000022140

Other devices from Ceren Üreti̇m Plasti̇k Ürünleri̇ Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇

Artimed

Class IIa
Ceren

Class I
Ccmed

Class I
Exxe

Class I
cerenüretim

Class I
Artimed

Class IIa

See all devices from Ceren Üreti̇m Plasti̇k Ürünleri̇ Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇ →

Properties

Other properties (11)

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