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U2 Knee Modular Disposable Trial

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 2104-2265

by United Orthopedic Corporation

Identity

Trade Name
U2 Knee Modular Disposable Trial EUDAMED
U2™ Knee FDA UDI
Generic Name
Knee femur prosthesis trial, reusable FDA UDI
Device Name
Femoral trial set, #6.5, right EUDAMEDFDA UDI
Model / Reference
2104-2265 EUDAMEDFDA UDI
Description
Femoral trial set, #6.5, right FDA UDI

Identifiers

Catalog Number
2104-2265 FDA UDI
Primary DI / UDI-DI
04711605579056 EUDAMEDFDA UDI
Basic UDI-DI
B-04711605579056 EUDAMED
510(k) Number
K120507 FDA UDI
K131116 FDA UDI
K131864 FDA UDI
K132752 FDA UDI
K140073 FDA UDI
K140075 FDA UDI
K150829 FDA UDI
K150832 FDA UDI
K152430 FDA UDI
K161360 FDA UDI
K161705 FDA UDI
FDA Product Code
OIY FDA UDI
MBH FDA UDI
JWH FDA UDI
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Knee femur prosthesis trial, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
888.3560 FDA UDI
888.3565 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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

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

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 1a87e8cf-f136-4beb-8c63-303eb2504ad7 61 fields · synced Jul 10, 2026
  • FDA UDI a609ec3c-8765-4532-acc3-0e52b799dfc5 37 fields · synced May 24, 2026