eudamed_udi Primary ID: 06951467490061

POLYMED (UDI 06951467490061)

Manufactured by Ningbo Boya Medical Equipment Co., Ltd

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

Scannable UDI-DI Representation

Device Regulatory Overview

The POLYMED (Model/Catalog Number: GZ-GL-4) is a medical device manufactured by Ningbo Boya Medical Equipment Co., Ltd. This product is indexed under FDA Product Code / Category Classification R040101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: GZ-GL-4
Product Code / EMDN: R040101
Device Name: GZ-GL-1/GZ-GL-2/GZ-GL-3/GZ-GL-3(A)/GZ-GL-3(B)/GZ-GL-4/GZ-GL-4(A)/GZ-GL-4(B)/GZ-GL-5/GZ-GL-5(A)/GZ-GL-5(B)/GZ-GL-6/GZ-GL-7/GZ-GL-8/GZ-GL-9
Database Sync Date: 2026-08-09 16:50:05

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 POLYMED?

The registered manufacturer of record for POLYMED is Ningbo Boya Medical Equipment Co., Ltd.

What is the Primary UDI-DI identifier for POLYMED?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06951467490061.

What classification code is assigned to this device?

This device is registered under product classification code R040101.

Similar Classification Devices (R040101)

Other Devices by Ningbo Boya Medical Equipment Co., Ltd

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