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USTAR II Hip System

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 9115-4001

by United Orthopedic Corporation

Identity

Trade Name
USTAR II Hip System EUDAMEDFDA UDI
Generic Name
Bone-resection orthopaedic reamer, reusable FDA UDI
Device Name
USTAR II Press-fit stem barrel reamer EUDAMEDFDA UDI
Model / Reference
9115-4001 EUDAMEDFDA UDI
Description
USTAR II Press-fit stem barrel reamer FDA UDI

Identifiers

Primary DI / UDI-DI
04719872140207 EUDAMEDFDA UDI
Basic UDI-DI
B-04719872140207 EUDAMED
FDA Product Code
HTO FDA UDI
EMDN Code
L091102 ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE EUDAMED
GMDN Term
Bone-resection orthopaedic reamer, 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

USTAR II 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 8fffeb34-6ef0-4683-a684-11fe29954b07 61 fields · synced Jul 12, 2026
  • FDA UDI e9ebb2f1-4537-4056-ade3-e47c46951f05 34 fields · synced May 30, 2026