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BioFiber

EUDAMED

Class IIb (EU MDR)

Ref BF-2BSTModel Nonabsorbable Soft Tissue & Bone Fixation Device - Sutures and Tapes

by Chetan Meditech Pvt. Ltd.

Identity

Trade Name
BioFiber EUDAMED
Device Name
BIOTEK, BioFiber EUDAMED
Model / Reference
Nonabsorbable Soft Tissue & Bone Fixation Device - Sutures and Tapes EUDAMED
BF-2BST EUDAMED

Identifiers

Primary DI / UDI-DI
18904210301300 EUDAMED
Basic UDI-DI
89042103cmplimp007XK EUDAMED
EMDN Code
H0102010299 SYNTHETIC NONABSORBABLE MULTIFILAMENT SUTURES - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Greece 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

Category: Polyester suture, non-bioabsorbable, multifilament

BioFiber by Chetan Meditech Pvt. Ltd. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Polyester suture, non-bioabsorbable, multifilament.

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 e045c552-26a2-415d-91d6-93ff103b9db7 61 fields · synced Jun 19, 2026