eudamed_udi Primary ID: 06973113121914

Zinc oxide plaster (UDI 06973113121914)

Manufactured by XIAMEN TICARE IMP.&EXP. CO., LTD.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Zinc oxide plaster (Model/Catalog Number: 7.5cmx5m) is a medical device manufactured by XIAMEN TICARE IMP.&EXP. CO., LTD.. This product is indexed under FDA Product Code / Category Classification M03020201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 7.5cmx5m
Product Code / EMDN: M03020201
Device Name: Zinc oxide plaster
Database Sync Date: 2026-08-09 19:07:09

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 Zinc oxide plaster?

The registered manufacturer of record for Zinc oxide plaster is XIAMEN TICARE IMP.&EXP. CO., LTD..

What is the Primary UDI-DI identifier for Zinc oxide plaster?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973113121914.

What classification code is assigned to this device?

This device is registered under product classification code M03020201.

Similar Classification Devices (M03020201)

Other Devices by XIAMEN TICARE IMP.&EXP. CO., LTD.

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