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Delta Dual Mobility System

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
Delta Dual Mobility System FDA UDI
Generic Name
Ceramic acetabular liner FDA UDI
Device Name
Liner #L for Mobile Liner Dia. 42 mm FDA UDI
Model / Reference
5885.09.042 FDA UDI
Description
Liner #L for Mobile Liner Dia. 42 mm FDA UDI

Identifiers

Catalog Number
5885.09.042 FDA UDI
Primary DI / UDI-DI
08033390020060 FDA UDI
FDA Product Code
LZO FDA UDI
LPH FDA UDI
MBL FDA UDI
GMDN Term
Ceramic acetabular liner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3358 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: Ceramic acetabular liner

Delta Dual Mobility System by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ceramic acetabular liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI 95d91e3a-5882-4b0e-9017-ac65626cc32f 35 fields · synced May 30, 2026