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Meg-Torq

EUDAMEDFDA 510(k)

Class IIa (EU MDR)

Ref MEG-TORQ

by MICRO-NX Co., Ltd.

Identity

Model / Reference
MEG-TORQ EUDAMED

Identifiers

Primary DI / UDI-DI
08800029600142 EUDAMED
Basic UDI-DI
B-08800029600142 EUDAMED
EMDN Code
Q010399 SURGICAL DENTAL DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Meg-Torq by MICRO-NX Co., Ltd. — Class IIa — FDA_510K, MDD — listed in EUDAMED, FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDD

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Manufacturer

Manufacturer
MICRO-NX Co., Ltd.
EUDAMED SRN
KR-MF-000026311
Authorised Representative
Javitech Consulting GmbH DE-AR-000045915

Sources (2)

  • EUDAMED 4e3f8bef-49ed-4ce1-b3b3-63275fafadfd 61 fields · synced Jun 18, 2026
  • FDA 510(k) K161500 1 fields · synced May 18, 2026