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Surgi-ORC

EUDAMED

Class III (EU MDR)

Ref SOO, SOK, SON, SOFModel Original/Standard, Knit, Fibril, Non-woven/Snow

by Aegis Lifesciences Pvt. Ltd.

Identity

Trade Name
Surgi-ORC EUDAMED
Device Name
Oxidized Regenerated Cellulose Haemostat EUDAMED
Model / Reference
Original/Standard, Knit, Fibril, Non-woven/Snow EUDAMED
SOO, SOK, SON, SOF EUDAMED

Identifiers

Primary DI / UDI-DI
D-890603845ORCQU EUDAMED
Basic UDI-DI
B-890603845ORCQU EUDAMED
EMDN Code
M040404 CELLULOSE AND/OR MODIFIED CELLULOSE DRESSINGS, NON-COMBINED OR COMBINED WITH OTHER SUBSTANCES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Norway 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

Surgi-ORC by Aegis Lifesciences Pvt. 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
IN-MF-000024058
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED 693a706e-baf4-4d1c-b8a1-f81269beeadb-1 61 fields · synced Jul 13, 2026
  • EUDAMED 693a706e-baf4-4d1c-b8a1-f81269beeadb-2 61 fields · synced Jul 13, 2026