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V9099

EUDAMED

Class I (EU MDR)

Ref K-LT57Model K-ET625,K-ET625A,K-ET625A1,K-ET625A2,K-ET625B,K-ET625C,K-ET625F,K-ET625E, K-ET750,K-ET750A,K-ET750A1,K-ET750A2,K-ET750B,K-ET750C,K-ET750F,K-ET750E, K-ET850,K-ET850A,K-ET850A1,K-ET850A2,K-ET850B, etc

by Chaozhou Yuhua Medical Device Technology Co., Ltd

Identity

Device Name
V9099 EUDAMED
Model / Reference
K-ET625,K-ET625A,K-ET625A1,K-ET625A2,K-ET625B,K-ET625C,K-ET625F,K-ET625E, K-ET750,K-ET750A,K-ET750A1,K-ET750A2,K-ET750B,K-ET750C,K-ET750F,K-ET750E, K-ET850,K-ET850A,K-ET850A1,K-ET850A2,K-ET850B, etc EUDAMED
K-LT57 EUDAMED

Identifiers

Primary DI / UDI-DI
06979192302176 EUDAMED
Basic UDI-DI
697919230MT001LK EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

The V9099 medical device from Chaozhou Yuhua Medical Device Technology Co., Ltd is a Class I implantable device, designed for treating various conditions. This European-approved device has been approved under the standard regulatory framework and meets high safety standards. It's essential to consult with a healthcare professional before using any device.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Chaozhou Yuhua Medical Device Technology Co., Ltd
EUDAMED SRN
CN-MF-000049992
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 5295da05-16f8-4ccd-a525-11597998d3d1 61 fields · synced Oct 9, 2026