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Ovis Cog

EUDAMED

Class III (EU MDR)

Ref F-LL 19G38(2)Model F-LL19G38(2)Ref L-LL19G38(2)

by Ovistech Co., Ltd.

Identity

Trade Name
OVIS COG EUDAMED
Device Name
Sterile single use absorbable polydioxanone suture with needle EUDAMED
Model / Reference
F-LL19G38(2) EUDAMED
F-LL 19G38(2) EUDAMED
L-LL19G38(2) EUDAMED

Identifiers

Primary DI / UDI-DI
08800056900000 EUDAMED
08800056900017 EUDAMED
Basic UDI-DI
B-08800056900000 EUDAMED
B-08800056900017 EUDAMED
EMDN Code
H010101010104 MOUNTED POLYDIOXANONE MONOFILAMENT WITH NEEDLE FOR TISSUE TRACTION (‘BARBED’) EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Latvia EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMEDEUDAMED

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

Ovis Cog by Ovistech 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

Manufacturer
Ovistech Co., Ltd.
EUDAMED SRN
KR-MF-000019873
Authorised Representative
JaviTech e.K. DE-AR-000005875

Sources (2)

  • EUDAMED ba4cc460-53fe-424f-a8b4-4d916eafb038 61 fields · synced Jul 16, 2026
  • EUDAMED 7908b487-e6da-41ea-a3a8-c94438f974ff 61 fields · synced May 18, 2026