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CoCrMo Alloy Femoral Heads 12/14

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 0520282Model Co-Cr-Mo FEMORAL HEAD CONE 12/14 DIAM 28 MEDIUM

by Adler Ortho Spa

Identity

Trade Name
CO-CR HEADS EUDAMED
CoCrMo Alloy Femoral Heads 12/14 FDA UDI
Generic Name
Metallic femoral head prosthesis FDA UDI
Device Name
CoCrMo Femoral Head Ø28mm (Medium) FDA UDI
Model / Reference
Co-Cr-Mo FEMORAL HEAD CONE 12/14 DIAM 28 MEDIUM EUDAMED
0520282 EUDAMED
Femoral Head FDA UDI
Description
CoCrMo Femoral Head Ø28mm (Medium) FDA UDI

Identifiers

Catalog Number
0520282 FDA UDI
Primary DI / UDI-DI
08052532831432 EUDAMEDFDA UDI
Basic UDI-DI
B-08052532831432 EUDAMED
FDA Product Code
LPH FDA UDI
JDI FDA UDI
LZO FDA UDI
MBL FDA UDI
EMDN Code
P090804050202 METAL FEMORAL HEADS, TOTAL HIP REPLACEMENT EUDAMED
GMDN Term
Metallic femoral head prosthesis FDA UDI

Classification

Device Class
Class III EUDAMED
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3350 FDA UDI
888.3353 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Metallic femoral head prosthesis

CoCrMo Alloy Femoral Heads 12/14 by Adler Ortho Spa — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Metallic femoral head prosthesis.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Adler Ortho Spa

Sources (2)

  • FDA UDI 57f805d2-fc65-48b7-9f20-3d03e19f79c0 35 fields · synced Jun 19, 2026
  • EUDAMED c319a98f-4cd2-42d0-8232-27caf1ecf198 61 fields · synced Jun 19, 2026