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Reflecto Femoral Augment Distal L.l./R.m Size 5 X 8 Mm

EUDAMED

Class III (EU MDR)

Ref 01.9841Model REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 5 X 8 MMRef 01.9829Model REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 5 X 4 MM

by Covision Medical Technologies Ltd.

Identity

Trade Name
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 5 X 8 MM EUDAMED
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 5 X 4 MM EUDAMED
Device Name
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 5 X 8 MM EUDAMED
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 5 X 4 MM EUDAMED
Model / Reference
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 5 X 8 MM EUDAMED
01.9841 EUDAMED
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 5 X 4 MM EUDAMED
01.9829 EUDAMED

Identifiers

Primary DI / UDI-DI
05051659178171 EUDAMED
05051659178058 EUDAMED
Basic UDI-DI
B-05051659178171 EUDAMED
B-05051659178058 EUDAMED
EMDN Code
P09098001 KNEE PROSTHESES AUGMENTS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Austria 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

Reflecto Femoral Augment Distal L.l./R.m Size 5 X 8 Mm by Covision Medical Technologies Ltd. — Class III — MDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
GB-MF-000025081
Authorised Representative
Covision Medical Technologies (Ireland) Limited IE-AR-000031129

Sources (2)

  • EUDAMED 9728c883-cd4c-4cce-89cf-57296fcd1933 61 fields · synced Oct 7, 2026
  • EUDAMED 7c539d8f-6586-4857-8ba0-332368caf102 61 fields · synced May 18, 2026