← Back to catalogue

U2 Total Knee System

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 9403-3004

by United Orthopedic Corporation

Identity

Trade Name
U2 Total Knee System EUDAMEDFDA UDI
Generic Name
Fluted surgical drill bit, reusable FDA UDI
Device Name
Tibial stem drill, 20mm EUDAMEDFDA UDI
Model / Reference
9403-3004 EUDAMEDFDA UDI
Description
Tibial stem drill, 20mm FDA UDI

Identifiers

Catalog Number
9403-3004 FDA UDI
Primary DI / UDI-DI
04711605584838 EUDAMEDFDA UDI
Basic UDI-DI
B-04711605584838 EUDAMED
FDA Product Code
HTW FDA UDI
EMDN Code
L091102 ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE EUDAMED
GMDN Term
Fluted surgical drill bit, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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

Category: Acetabular orthopaedic reamer

U2 Total Knee System by United Orthopedic Corporation — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acetabular orthopaedic reamer.

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 13bfa503-03f9-4b7c-94f4-e46cff50df89 61 fields · synced Jul 9, 2026
  • FDA UDI cb01c6a0-6ade-48de-8a57-6b2e282c5977 35 fields · synced May 26, 2026