← Back to catalogue

Biotek

EUDAMED

Class I (EU MDR)

Ref BAK-7062Model 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
BAK-7062 EUDAMED

Identifiers

Primary DI / UDI-DI
18904210398072 EUDAMED
Basic UDI-DI
89042103cmplins006YH EUDAMED
EMDN Code
L1999 ARTHROSCOPIC SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 553abe4b-15dc-4261-a8c2-1373555e6356 61 fields · synced Jun 19, 2026