eudamed_udi Primary ID: 06903053093828

AngiotensinⅠ(CLIA) (UDI 06903053093828)

Manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AngiotensinⅠ(CLIA) (Model/Catalog Number: 105-049536-00) is a medical device manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102060202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 105-049536-00
Product Code / EMDN: W0102060202
Device Name: AngiotensinⅠ(CLIA)
Database Sync Date: 2026-08-09 16:44:54

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 AngiotensinⅠ(CLIA)?

The registered manufacturer of record for AngiotensinⅠ(CLIA) is Shenzhen Mindray Bio-Medical Electronics Co., Ltd..

What is the Primary UDI-DI identifier for AngiotensinⅠ(CLIA)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06903053093828.

What classification code is assigned to this device?

This device is registered under product classification code W0102060202.

Similar Classification Devices (W0102060202)

Other Devices by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

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