← Back to catalogue

UTS Hip Stem

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 9116-2001

by United Orthopedic Corporation

Identity

Trade Name
UTS Hip Stem EUDAMEDFDA UDI
Generic Name
Osteotomy guide, reusable FDA UDI
Device Name
United Hip and Knee Non-sterile Reusable Instruments EUDAMED
UTS Neck resection guide FDA UDI
Model / Reference
9116-2001 EUDAMEDFDA UDI
Description
UTS Neck resection guide FDA UDI

Identifiers

Catalog Number
9116-2001 FDA UDI
Primary DI / UDI-DI
04711605582223 EUDAMEDFDA UDI
Basic UDI-DI
471987216TD-Ir-003F4 EUDAMED
Direct Marketing DI
04711605582223 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Osteotomy guide, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA 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

UTS 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

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 e554ef2e-47a7-4e55-9eb4-3f370d0788c7 61 fields · synced Jun 9, 2026
  • FDA UDI 47ee2ae8-172c-49b7-8822-6a6f92fa05f7 35 fields · synced May 30, 2026