Prophecy

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name: PROPHECY FDA UDI
Generic Name: Joint prosthesis implantation kit, reusable FDA UDI
Model / Reference: PNV04179 FDA UDI

Identifiers

Catalog Number: PNV04179 FDA UDI
Primary DI / UDI-DI: M684PNV041791 FDA UDI
FDA Product Code: MBH FDA UDI
JWH FDA UDI
OOG FDA UDI
GMDN Term: Joint prosthesis implantation kit, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3565 FDA UDI
888.3560 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

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

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Also classified as Joint prosthesis implantation kit, reusable.

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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 936a2b94-df7b-4830-8fba-387747757087 34 fields · synced Jun 9, 2026