Medippro

by MEDICAL IP Co., Ltd.

Ref MEDIP Pro V2.0 User Manual (2024.03 Revision 1.0.0)

Active European Union and United States

CE MDD 510(k)

Valid until

Not listed

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K191026↗

FDA record

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, FDA 510(k), 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 EUDAMED	NumberB-08809590100006 Basic UDI-DI 08809590100006UDI-DI	Date16 Jun 2025Registered	StatusActive
United States	FDA 510(k) 510(k)	NumberK191026	Date7 Nov 2019Issued	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.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

2 jurisdictions

Active
Expiring
Withdrawn
Listed
Not covered

United States FDA 510(k) Active
European Union CE/MDD Active

Specification

EUDAMED · 510(k)

Model / Reference: MEDIP Pro V2.0 User Manual (2024.03 Revision 1.0.0)

Primary DI / UDI-DI: 08809590100006
Basic UDI-DI: B-08809590100006
EMDN Code: Z11900801 Bioimaging diagnostic report viewing monitors

Device Class: Class IIa
Special Device Type: -1192
EU market of registration: Northern Ireland

Manufacturer details

EUDAMED SRN: KR-MF-000013954
Authorised representative: Advena Limited MT-AR-000000234

Other devices from MEDICAL IP Co., Ltd.

DeepCatch

Class II

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