← Back to catalogue

Reflecto Femoral Augment Distal L.l./R.m Size 4 X 4 Mm

EUDAMED

Class III (EU MDR)

Ref 01.9827Model REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 4 X 4 MMRef 01.9839Model REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 4 X 8 MM

by Covision Medical Technologies Ltd.

Identity

Trade Name
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 4 X 4 MM EUDAMED
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 4 X 8 MM EUDAMED
Device Name
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 4 X 4 MM EUDAMED
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 4 X 8 MM EUDAMED
Model / Reference
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 4 X 4 MM EUDAMED
01.9827 EUDAMED
REFLECTO FEMORAL AUGMENT DISTAL L.L./R.M SIZE 4 X 8 MM EUDAMED
01.9839 EUDAMED

Identifiers

Primary DI / UDI-DI
05051659178034 EUDAMED
05051659178157 EUDAMED
Basic UDI-DI
B-05051659178034 EUDAMED
B-05051659178157 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 4 X 4 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED beac564d-4997-41fe-8bce-670f98d230a0 61 fields · synced Oct 6, 2026
  • EUDAMED 48ea5d21-88b8-4fca-8ad3-5c0eac3bdc65 61 fields · synced May 17, 2026