Ureteral Stent Package

by Hunan Reborn Medical Science and Technology Development Co., Ltd 1,000+ variants

Model F3,F4,F4.7,F4.8,F5,F6,F7,F8

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-CNMF000023648USP17693W2 Basic UDI-DI D-CNMF000023648USP17693W2UDI-DI	Date1 Aug 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Withdrawn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

Model / Reference: F3, F4, F4.7, F4.8, F5, F6, F7, F8

Primary DI / UDI-DI: D-CNMF000023648USP17693W2
Basic UDI-DI: B-CNMF000023648USP17693W2
EMDN Code: U020302 Double loop ureteral stents

Device Class: Class IIa
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: CN-MF-000023648
Authorised representative: MedPath GmbH DE-AR-000000087

Other devices from Hunan Reborn Medical Science and Technology Development Co., Ltd

Disposable Digital Flexible Ureteroscope

Class IIa
Ureteral Stent Package

Class IIa
Ureteral Access Sheath

Class IIa
Hydrophilic Silicone Foley Catheter

Class IIa
Zebra Guidewire

Class IIa
Ureteral Stent Package

Class IIa

See all devices from Hunan Reborn Medical Science and Technology Development Co., Ltd →

Properties

Sterile

Other properties (10)

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