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U2 Total Knee System

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 2803-6121

by United Orthopedic Corporation

Identity

Trade Name
U2 Total Knee System EUDAMED
U2™ Knee FDA UDI
Generic Name
Knee tibia prosthesis trial, reusable FDA UDI
Device Name
Tibial augment trial, #2, 5mm, left EUDAMEDFDA UDI
Model / Reference
2803-6121 EUDAMEDFDA UDI
Description
Tibial augment trial, #2, 5mm, left FDA UDI

Identifiers

Catalog Number
2803-6121 FDA UDI
Primary DI / UDI-DI
04719872166450 EUDAMEDFDA UDI
Basic UDI-DI
B-04719872166450 EUDAMED
510(k) Number
K122183 FDA UDI
K161360 FDA UDI
K161705 FDA UDI
FDA Product Code
MBH FDA UDI
JWH FDA UDI
OIY FDA UDI
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Knee tibia prosthesis trial, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
888.3565 FDA UDI
888.3560 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

U2 Total 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 b6c83336-88c7-4131-b833-6de0282e5ca2 61 fields · synced Jun 9, 2026
  • FDA UDI fdb90fc0-5e7d-4443-8ecf-98166d2b08b5 37 fields · synced May 30, 2026