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Bio-Vim

EUDAMED

Class III (EU MDR)

Ref 10075Model Bioabsorbable Soft Tissue & Bone Fixation Devices - Bone and Suture Anchor

by Chetan Meditech Pvt. Ltd.

Identity

Trade Name
BIO-VIM EUDAMED
Device Name
BIOTEK, BIO-VIM, BIO-VIM LRP, BIO-VIM LRT, ARTHROVIMS BR Anchor EUDAMED
Model / Reference
Bioabsorbable Soft Tissue & Bone Fixation Devices - Bone and Suture Anchor EUDAMED
10075 EUDAMED

Identifiers

Primary DI / UDI-DI
18904210302239 EUDAMED
Basic UDI-DI
89042103cmplimp001X7 EUDAMED
EMDN Code
P09120102 ANCHORS, TENDON AND LIGAMENT SYNTHESIS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

Category: Hand-held surgical retractor, reusable

Bio-Vim by Chetan Meditech Pvt. Ltd. — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held surgical retractor, reusable.

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 3fcbe861-20c7-4cf4-ab93-02b3f0d0ccfe 61 fields · synced Jun 17, 2026