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T Hole-In

EUDAMED

Class I (EU MDR)

Ref FP1035THModel T Hole-In

by Nexobio Co., Ltd.

Identity

Device Name
T Hole-In EUDAMED
Model / Reference
T Hole-In EUDAMED
FP1035TH EUDAMED

Identifiers

Primary DI / UDI-DI
08800032400272 EUDAMED
Basic UDI-DI
88000324THAF EUDAMED
Unit of Use DI
08800032401804 EUDAMED
EMDN Code
Q0199 ODONTOLOGY DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye 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

T Hole-In by Nexobio Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Nexobio Co., Ltd.
EUDAMED SRN
KR-MF-000043543
Authorised Representative
MEGALİNE DENTAL İTH. İHR. SAN. TİC. LTD. ŞTİ. TR-AR-000046036

Sources (1)

  • EUDAMED 4d553ce6-fdc0-4b54-b0df-e954440cc710 61 fields · synced Jul 12, 2026