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UTF Hip Stem

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 9106-6303

by United Orthopedic Corporation

Identity

Trade Name
UTF Hip Stem EUDAMED
UTF™ Stem FDA UDI
Generic Name
Orthopaedic broach FDA UDI
Device Name
United Hip and Knee Non-sterile Reusable Instruments EUDAMED
UTF Broach, reduced, #3 FDA UDI
Model / Reference
9106-6303 EUDAMEDFDA UDI
Description
UTF Broach, reduced, #3 FDA UDI

Identifiers

Catalog Number
9106-6303 FDA UDI
Primary DI / UDI-DI
04719872167433 EUDAMEDFDA UDI
Basic UDI-DI
471987216TD-Ir-003F4 EUDAMED
Direct Marketing DI
04719872167433 EUDAMED
510(k) Number
K123550 FDA UDI
K132207 FDA UDI
K132455 FDA UDI
FDA Product Code
MEH FDA UDI
LWJ FDA UDI
KWY FDA UDI
LPH FDA UDI
LZO FDA UDI
EMDN Code
L091202 ORTHOPAEDIC SURGERY FILES, REUSABLE EUDAMED
GMDN Term
Orthopaedic broach FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3360 FDA UDI
888.3390 FDA UDI
888.3358 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

UTF Hip Stem by United Orthopedic Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

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 7209c372-0c50-4a04-9e57-7398998d92e1 61 fields · synced Jul 10, 2026
  • FDA UDI 996c7cb9-2a2f-446a-b848-914df13bd535 37 fields · synced May 30, 2026