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UIMD Inc.

Active in EUDAMED

South Koreafrom SRN EUDAMED SRN KR-MF-000034633

Devices
3
Registrations
EUDAMED

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
Authorised rep.
MDSS GmbHDE

What UIMD Inc. makes

UIMD Inc. manufactures medical devices identified as PBIA-12A and PBIA-100A. These products fall under the Class A device category, indicating a lower risk profile. The company is based in South Korea and focuses on producing these specific device models.

The portfolio is regulated under Class A device classifications and is listed in the eudamed registry. The manufacturer is located in South Korea. Individual devices are authorised according to their respective regulatory requirements.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • CELL i-1A

    Class A
    Active CE IVDR EUDAMED A
  • Pbia-12A

    Class A
    Active CE IVDR EUDAMED A
  • Pbia-100A

    Class A
    Active CE IVDR EUDAMED A

Company details

EUDAMED SRN
KR-MF-000034633
EUDAMED status
Active
EUDAMED registered name
UIMD Inc.
Registered address
15, Mallijae-ro, 04214, Seoul, South Korea
Phone
+821062963277
PRRC contact
wonseok Choi(public in EUDAMED)

Frequently asked questions

How many devices does UIMD Inc. have in the registry?

The registry currently lists 3 devices for UIMD Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list UIMD Inc.'s devices?

Among its 3 most recently registered devices, UIMD Inc. has devices listed in EUDAMED (3 devices).

What risk classes do UIMD Inc.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for UIMD Inc.'s devices are IVDR Class A. Each device page shows its own class and authorisation.

What are the newest devices from UIMD Inc. in the registry?

The most recently registered devices listed for UIMD Inc. include CELL i-1A, PBIA-12A and PBIA-100A.

Generated automatically from registry data and not verified by a human reviewer.