Implant Partners

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name: Implant Partners FDA UDI
Generic Name: Press-fit hip femur prosthesis, one-piece FDA UDI
Device Name: TL PLASMA VAR8 SHORT SIZE 9 IMPLANT PARTNERS™ FDA UDI
Model / Reference: PRTLE029WD FDA UDI
Description: TL PLASMA VAR8 SHORT SIZE 9 IMPLANT PARTNERS™ FDA UDI

Identifiers

Catalog Number: PRTLE029WD FDA UDI
Primary DI / UDI-DI: M684PRTLE029WD1 FDA UDI
FDA Product Code: LZO FDA UDI
JDI FDA UDI
GMDN Term: Press-fit hip femur prosthesis, one-piece FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3353 FDA UDI
888.3350 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

Category: Press-fit hip femur prosthesis, one-piece

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

Similar devices

Also classified as Press-fit hip femur prosthesis, one-piece.

Masterloc Femoral Stems — Medacta International · Class II
Paragon — GLOBAL MANUFACTURING TECHNOLOGY PTY LIMITED · Class II
AMIStem H Femoral Stems — Medacta International · Class II
Quadra H femoral stems — Medacta International · Class II
Amis K Long femoral stems — Medacta International · Class II
Klassic Blade Femoral Stem, Porous, Size 1 — TOTAL JOINT ORTHOPEDICS, INC. · Class II
AMIStem-H Proximal Coating — Medacta International · Class II
Trivicta — ORTHO DEVELOPMENT CORP. · 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: MicroPort Orthopedics Inc.

Sources (1)

FDA UDI b21f0187-70e2-4dfd-905a-a86fd75cfcf3 35 fields · synced Jun 9, 2026