Extender

by İnvamed Sağlik İlaç Sanayi̇ Ve Ti̇caret A.Ş. 247 variants

Ref BTK50220S

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-8683498152417EX Basic UDI-DI D-8683498152417EXUDI-DI	Date10 Jul 2023Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name: Extender Drug-Released PTA 14 BTK Balloon Catheter, 5.0 mm Balloon diameter, 220 mm Balloon lenght,120 cm Catheter lenght
Model / Reference: BTK50220S

Primary DI / UDI-DI: D-8683498152417EX
Basic UDI-DI: B-8683498152417EX
EMDN Code: C010402020101 PTA balloon dilatation catheters

Device Class: Class III
EU market of registration: Türkiye

Manufacturer details

EUDAMED SRN: TR-MF-000019963

Other devices from İnvamed Sağlik İlaç Sanayi̇ Ve Ti̇caret A.Ş.

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Class III
Atlas

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Class III
Extender

Class III
Stena

Class III
İnvamed

Class IIb

See all devices from İnvamed Sağlik İlaç Sanayi̇ Ve Ti̇caret A.Ş. →

Properties

Sterile

Other properties (10)

Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No