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Biotek

EUDAMED

Class IIb (EU MDR)

Ref BAL-26.30.FHModel Nonabsorbable Soft Tissue & Bone Fixation Device - Soft Tissue & Bone Fixation Screw

by Chetan Meditech Pvt. Ltd.

Identity

Trade Name
BIOTEK EUDAMED
Device Name
BIOTEK, SOFTFIX, SOFTFIX-PK EUDAMED
Model / Reference
Nonabsorbable Soft Tissue & Bone Fixation Device - Soft Tissue & Bone Fixation Screw EUDAMED
BAL-26.30.FH EUDAMED

Identifiers

Primary DI / UDI-DI
18904210301652 EUDAMED
Basic UDI-DI
89042103cmplimp006XH EUDAMED
EMDN Code
P09120602,P09120603 EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

Yes

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 IIb — 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 1af45fb1-1802-4856-9eec-b49fd12be750 61 fields · synced Jul 10, 2026