Lineage

FDA UDI

Class III (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name: Lineage FDA UDI
Generic Name: Ceramic acetabular liner FDA UDI
Device Name: LINEAGE® CERAMIC LINER 32mm X 58-62mm GROUP 3 FDA UDI
Model / Reference: 73003258 FDA UDI
Description: LINEAGE® CERAMIC LINER 32mm X 58-62mm GROUP 3 FDA UDI

Identifiers

Catalog Number: 73003258 FDA UDI
Primary DI / UDI-DI: M684730032581 FDA UDI
FDA Product Code: MRA FDA UDI
GMDN Term: Ceramic acetabular liner FDA UDI

Classification

Device Class: Class III 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Lumen/Inner Diameter — 32 Millimeter FDA UDI

Category: Ceramic acetabular liner

Lineage by MicroPort Orthopedics Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ceramic acetabular liner.

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R3 ACETABULAR — Smith & Nephew, Inc. · Class III
R3 ACETABULAR — Smith & Nephew, Inc. · Class III
R3 ACETABULAR — Smith & Nephew, Inc. · Class III
BIRMINGHAM HIP — Smith & Nephew, Inc. · Class II
CERAMAX — DEPUY ORTHOPAEDICS, INC. · Class III

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

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Manufacturer

Manufacturer: MicroPort Orthopedics Inc.

Sources (1)

FDA UDI e1363aa4-07bc-4c3e-836f-83a952e7b239 36 fields · synced Jun 9, 2026