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DAOL MED Co., Ltd.

South Korea KR-MF-000026363 Last updated 17 Sep 2026

Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

  • Cellina Ref DC-1

    Class IIa EUDAMED Active

What DAOL MED Co., Ltd. makes

DAOL MED Co., Ltd. manufactures CELLINA, a medical device designed for cellular analysis or treatment procedures, though specific applications are not detailed.

The CELLINA device is classified as Class IIa under EU regulations and is registered in the EU’s eudamed database. The company is based in South Korea.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does DAOL MED Co., Ltd. manufacture?

DAOL MED Co., Ltd. manufactures the CELLINA device, which is designed for cellular analysis or treatment procedures. The exact applications are not specified, but the device falls under medical technology used in cellular interventions.

Where is DAOL MED Co., Ltd. based?

DAOL MED Co., Ltd. is based in South Korea. The company’s location is relevant for understanding its regulatory context and operational base.

Which regulatory registries list DAOL MED Co., Ltd.’s devices?

The CELLINA device from DAOL MED Co., Ltd. is listed in the eudamed database, which is the EU’s centralised registry for medical devices. This registry is used to track devices authorised under EU regulations.

How are DAOL MED Co., Ltd.’s devices classified under EU regulations?

The CELLINA device is classified as Class IIa under EU medical device regulations. This classification is determined by factors like the device’s intended purpose, risk level, and potential impact on patient safety, influencing its regulatory requirements.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
South Korea
Address
166beon-gil, 46, Galmaesunhwan-ro, Guri-si, Gyeonggi-do, South Korea
Phone
+82-26925-2199
PRRC contact
Sanghoon Choi
EUDAMED SRN
KR-MF-000026363