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U1 Total Hip System

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 9203-1201-RA

by United Orthopedic Corporation

Identity

Trade Name
U1 Total Hip System EUDAMED
U1™ Hip FDA UDI
Generic Name
Orthopaedic reamer handle FDA UDI
Device Name
Cup reamer handle EUDAMEDFDA UDI
Model / Reference
9203-1201-RA EUDAMEDFDA UDI
Description
Cup reamer handle FDA UDI

Identifiers

Catalog Number
9203-1201-RA FDA UDI
Primary DI / UDI-DI
04719872173038 EUDAMEDFDA UDI
Basic UDI-DI
B-04719872173038 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
L091102 ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE EUDAMED
GMDN Term
Orthopaedic reamer handle 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

U1 Total Hip 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

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Manufacturer

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

Sources (2)

  • EUDAMED 041d4e4a-3024-47be-9cd9-10d336c539ec 61 fields · synced Jul 24, 2026
  • FDA UDI 1145f0ed-61b4-41c6-bc62-66b2e285bea5 35 fields · synced May 30, 2026