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Biotek

EUDAMED

Class I (EU MDR)

Ref 10721Model Non Invasive Arthroscopy and Orthopaedic Instruments

by Chetan Meditech Pvt. Ltd.

Identity

Trade Name
BIOTEK EUDAMED
Device Name
BIOTEK EUDAMED
Model / Reference
Non Invasive Arthroscopy and Orthopaedic Instruments EUDAMED
10721 EUDAMED

Identifiers

Primary DI / UDI-DI
18904210393619 EUDAMED
Basic UDI-DI
89042103cmplins006YH EUDAMED
EMDN Code
L0903 ORTHOPAEDIC SURGERY HAMMERS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Greece 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

Biotek by Chetan Meditech Pvt. 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

EUDAMED SRN
IN-MF-000013541
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED c82ac258-165b-4e30-a27c-9dd433281491 61 fields · synced Jun 19, 2026