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OK-Strips

EUDAMED

Class IIa (EU MDR)

Ref OKS80H/2Model OK-S, OK-P Series

by Jaintek Co., Ltd.

Identity

Trade Name
OK-Strips EUDAMED
Device Name
OK-Strips, OK-Proxofile EUDAMED
Model / Reference
OK-S, OK-P Series EUDAMED
OKS80H/2 EUDAMED

Identifiers

Primary DI / UDI-DI
08800115201529 EUDAMED
Basic UDI-DI
88001152S-0001U3 EUDAMED
EMDN Code
Q010399 SURGICAL DENTAL DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

OK-Strips by Jaintek Co., Ltd. — Class IIa — 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
Jaintek Co., Ltd.
EUDAMED SRN
KR-MF-000045113
Authorised Representative
KTR Europe GmbH DE-AR-000005685

Sources (1)

  • EUDAMED 32087bfb-ddb7-4662-b4ff-f0b738c82ced 61 fields · synced Jun 19, 2026