← Back to catalogue

U2 Total Knee System

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 2303-2414-RF

by United Orthopedic Corporation

Identity

Trade Name
U2 Total Knee System EUDAMEDFDA UDI
Generic Name
Knee tibia prosthesis trial, reusable FDA UDI
Device Name
Tibial insert trial, UC, #1, 15mm EUDAMEDFDA UDI
Model / Reference
2303-2414-RF EUDAMEDFDA UDI
Description
Tibial insert trial, UC, #1, 15mm FDA UDI

Identifiers

Catalog Number
2303-2414-RF FDA UDI
Primary DI / UDI-DI
04719872163855 EUDAMEDFDA UDI
Basic UDI-DI
B-04719872163855 EUDAMED
510(k) Number
K132752 FDA UDI
FDA Product Code
JWH 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
888.3560 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

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

Manufacturer

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

Sources (2)

  • EUDAMED ea9bfaf9-fb46-4a3c-970c-3442e6872a9c 61 fields · synced Oct 6, 2026
  • FDA UDI fae087f8-1940-43c7-96a9-6f0432f9dfa3 37 fields · synced May 30, 2026