PROHEAL (UDI PMOVBT-CHRY-MP)

Manufactured by XIAMEN TAFT MEDICAL CO.,LTD.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The PROHEAL (Model/Catalog Number: PMOVBT-CHRY-MP) is a medical device manufactured by XIAMEN TAFT MEDICAL CO.,LTD.. This product is indexed under FDA Product Code / Category Classification INW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PMOVBT-CHRY-MP
Product Code / EMDN: INW
Device Name
Database Sync Date: 2026-08-09 09:06:41

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of PROHEAL?

The registered manufacturer of record for PROHEAL is XIAMEN TAFT MEDICAL CO.,LTD..

What is the Primary UDI-DI identifier for PROHEAL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PMOVBT-CHRY-MP.

What classification code is assigned to this device?

This device is registered under product classification code INW.

Similar Classification Devices (INW)

Other Devices by XIAMEN TAFT MEDICAL CO.,LTD.

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