Medical Splint

by Anping Guardian Medical Equipment Co., Ltd 95 variants

Ref AZ-KBModel AZ-ST

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

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number697310523SplintFA Basic UDI-DI 06973105235209UDI-DI	Date12 Feb 2025Registered	StatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference: AZ-ST, AZ-KB

Primary DI / UDI-DI: 06973105235209
Basic UDI-DI: 697310523SplintFA
EMDN Code: M03050299 Bandages and splints - other

Device Class: Class I
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: CN-MF-000015025
Authorised representative: MedNet EC-REP GmbH DE-AR-000000002

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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