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Biotech Sterile Knee Endoprosthesis Systems

EUDAMED

Class III (EU MDR)

Ref 4049852KN1DNModel Biotech Sterile Knee Endoprosthesis Systems

by Biotech GmbH

Identity

Trade Name
Biotech Sterile Knee Endoprosthesis Systems EUDAMED
Device Name
Biotech Sterile Knee Endoprosthesis Systems EUDAMED
Model / Reference
Biotech Sterile Knee Endoprosthesis Systems EUDAMED
4049852KN1DN EUDAMED

Identifiers

Primary DI / UDI-DI
D-4049852KN1DNUB EUDAMED
Basic UDI-DI
B-4049852KN1DNUB EUDAMED
EMDN Code
P0909030101,P0909030102,P0909030103,P090903020101,P090903020102,P090903020103,P090903020104,P090903020105,P090903020106,P090903020201,P090903020202,P090903020301,P090903020399,P0909040101,P0909040102,P090904020101,P090904020102,P090904020103,P090904020104,P090904020201,P090904020202,P090904020301,P090904020302,P090904020401,P090904020499,P09090501,P090905020101,P090905020102,P090905020201,P090905020202,P090906,P09090701,P0909070201,P0909070202,P090908,P090999 EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Hungary 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

Biotech Sterile Knee Endoprosthesis Systems by Biotech GmbH — 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
Biotech GmbH
EUDAMED SRN
DE-MF-000023586

Sources (1)

  • EUDAMED 8ee31980-2c4d-4c7e-b061-98faa4ac0da2 61 fields · synced Jun 19, 2026