Microport

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name: MICROPORT FDA UDI
Generic Name: Joint prosthesis implantation kit, reusable FDA UDI
Device Name: FEMORAL HEAD TRIAL 40MM MEDIUM FDA UDI
Model / Reference: APA02140 FDA UDI
Description: FEMORAL HEAD TRIAL 40MM MEDIUM FDA UDI

Identifiers

Catalog Number: APA02140 FDA UDI
Primary DI / UDI-DI: 00192629100848 FDA UDI
FDA Product Code: LPH FDA UDI
LZO FDA UDI
JDI FDA UDI
GMDN Term: Joint prosthesis implantation kit, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3358 FDA UDI
888.3353 FDA UDI
888.3350 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

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

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Joint prosthesis implantation kit, reusable

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

Similar devices

Also classified as Joint prosthesis implantation kit, reusable.

Initia Total Hip System — Kyocera Corporation · Class II
Cadence Total Ankle System — Smith & Nephew, Inc. · Class I
G7 MINI TRAY — Biomet Orthopedics, Inc. · Class II
APEX Knee System — OMNIlife science, Inc. · Class I
Initia Total Hip System — Kyocera Corporation · Class I
APEX Knee System — OMNIlife science, Inc. · Class I
Engage Partial Knee System — Engage Uni, LLC · Class II
DFS — Biomet Orthopedics, Inc. · Class II

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 II	Pending data

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Manufacturer

Manufacturer: MicroPort Orthopedics Inc.

Sources (1)

FDA UDI d79ae9be-d9ea-45f3-bb7e-4ece01110dd6 35 fields · synced Jun 9, 2026