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Articul/Eze

FDA UDI

Class II (US FDA UDI)

by Depuy Orthopaedics, Inc.

Identity

Trade Name
ARTICUL/EZE FDA UDI
Generic Name
Ceramic femoral head prosthesis FDA UDI
Device Name
ARTICUL/EZE FEMORAL HEAD CERAMIC 12/14 TAPER 36mm plus 1.5 FDA UDI
Model / Reference
4734-36-015 FDA UDI
Description
ARTICUL/EZE FEMORAL HEAD CERAMIC 12/14 TAPER 36mm plus 1.5 FDA UDI

Identifiers

Catalog Number
473436015 FDA UDI
Primary DI / UDI-DI
10603295505709 FDA UDI
FDA Product Code
LZO FDA UDI
GMDN Term
Ceramic femoral head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Ceramic femoral head prosthesis

Articul/Eze by Depuy Orthopaedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ceramic femoral head prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2ff5555e-4904-42d8-93be-02637d8d2f1b 35 fields · synced Jun 8, 2026