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Lineage

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name
Lineage FDA UDI
Generic Name
Metallic acetabulum prosthesis FDA UDI
Device Name
LINEAGE® PC QUAD HEMI STD SHELL SIZE 46 GROUP 1 FDA UDI
Model / Reference
36510046 FDA UDI
Description
LINEAGE® PC QUAD HEMI STD SHELL SIZE 46 GROUP 1 FDA UDI

Identifiers

Catalog Number
36510046 FDA UDI
Primary DI / UDI-DI
M684365100461 FDA UDI
FDA Product Code
LPH FDA UDI
GMDN Term
Metallic acetabulum prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 46 Millimeter FDA UDI

Category: Metallic acetabulum prosthesis

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

Similar devices

Also classified as Metallic acetabulum prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 681da124-69bc-4db9-91d6-43ba989ac5d7 36 fields · synced Jun 9, 2026