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Reborn

EUDAMED

Class III (EU MDR)

Ref DS27038050I

by 21 Century Medical Co., Ltd.

Identity

Trade Name
Reborn EUDAMED
Device Name
Sterile single use polydioxanone Suture with needle EUDAMED
Model / Reference
DS27038050I EUDAMED

Identifiers

Primary DI / UDI-DI
08809822314799 EUDAMED
Basic UDI-DI
B-08809822314799 EUDAMED
EMDN Code
H010101010104 MOUNTED POLYDIOXANONE MONOFILAMENT WITH NEEDLE FOR TISSUE TRACTION (‘BARBED’) EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

Reborn by 21 Century Medical Co., Ltd. — Class III — 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
KR-MF-000009204
Authorised Representative
KTR Europe GmbH DE-AR-000005685

Sources (1)

  • EUDAMED bd22eda8-edd1-4661-9eb0-4070475a1afd 61 fields · synced Jun 18, 2026