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USTAR II Knee System

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 2115-4210

by United Orthopedic Corporation

Identity

Trade Name
USTAR II Knee System EUDAMEDFDA UDI
Generic Name
Knee femur prosthesis trial, reusable FDA UDI
Device Name
USTAR II Distal femoral trial, RHS, S, right EUDAMEDFDA UDI
Model / Reference
2115-4210 EUDAMEDFDA UDI
Description
USTAR II Distal femoral trial, RHS, S, right FDA UDI

Identifiers

Catalog Number
2115-4210 FDA UDI
Primary DI / UDI-DI
04719872140009 EUDAMEDFDA UDI
Basic UDI-DI
B-04719872140009 EUDAMED
510(k) Number
K190100 FDA UDI
FDA Product Code
KRO FDA UDI
LPH FDA UDI
LWJ FDA UDI
KWL FDA UDI
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Knee femur prosthesis trial, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
888.3510 FDA UDI
888.3358 FDA UDI
888.3360 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

USTAR II Knee System by United Orthopedic Corporation — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
TW-MF-000009523
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (2)

  • EUDAMED 53bd97a3-0f6c-4c7a-ad48-227318159c70 61 fields · synced Oct 7, 2026
  • FDA UDI 6fa144a6-26ef-4bc2-b8bd-6b11b4cdefda 36 fields · synced May 30, 2026