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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
Non-constrained polyethylene acetabular liner FDA UDI
Device Name
Mobile Liner Dia. 42 mm for Head Dia. 28 mm FDA UDI
Model / Reference
5566.50.420 FDA UDI
Description
Mobile Liner Dia. 42 mm for Head Dia. 28 mm FDA UDI

Identifiers

Catalog Number
5566.50.420 FDA UDI
Primary DI / UDI-DI
08033390012447 FDA UDI
FDA Product Code
LZO FDA UDI
LPH FDA UDI
MBL FDA UDI
GMDN Term
Non-constrained polyethylene 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: Non-constrained polyethylene 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 Non-constrained polyethylene 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 dd921bb9-7a4a-4d2f-87c3-2b7c8d67fd94 35 fields · synced Jun 1, 2026