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Maxipore

EUDAMED

Class I (EU MDR)

Ref S522

by Seyi̇tler Ki̇mya Sanayi̇ A.ş.

Identity

Trade Name
Maxipore EUDAMED
Device Name
Maxipore Nonwoven IV Cannula Fixer EUDAMED
Model / Reference
S522 EUDAMED

Identifiers

Primary DI / UDI-DI
08699664400015 EUDAMED
Basic UDI-DI
B-08699664400015 EUDAMED
EMDN Code
M04010102 POLYURETHANE (OR OTHER MATERIAL) ADHESIVE DRESSINGS, WITH ABSORBENT PAD EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Maxipore by Seyi̇tler Ki̇mya Sanayi̇ A.ş. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TR-MF-000019722

Sources (1)

  • EUDAMED 0ee03d17-477b-4985-a033-bfd14c7f08e5 61 fields · synced Jun 19, 2026