← Back to catalogue

Articul/Eze

FDA UDI

Class II (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
ARTICUL/EZE FDA UDI
Generic Name
Metallic femoral head prosthesis FDA UDI
Device Name
ARTICUL/EZE FEMORAL HEAD Diameter 32mm +17 12/14 TAPER FDA UDI
Model / Reference
1365-25-000 FDA UDI
Description
ARTICUL/EZE FEMORAL HEAD Diameter 32mm +17 12/14 TAPER FDA UDI

Identifiers

Catalog Number
136525000 FDA UDI
Primary DI / UDI-DI
10603295033219 FDA UDI
510(k) Number
K843909 FDA UDI
K883460 FDA UDI
FDA Product Code
JDI FDA UDI
GMDN Term
Metallic femoral head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3350 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

Category: Metallic femoral head prosthesis

Articul/Eze by Depuy (ireland) — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic femoral head prosthesis.

Cleared under the same submission

K843909 also covers:

K883460 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI 67526036-55b0-4408-936d-6cff97ab9704 36 fields · synced Jun 1, 2026