Angiotensin Converting Enzyme (ACE) Kit (Enzymatic Colorimetric Assay Method) (UDI 06944904053363)
Manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Device Regulatory Overview
The Angiotensin Converting Enzyme (ACE) Kit (Enzymatic Colorimetric Assay Method) (Model/Catalog Number: 105-004509-00) is a medical device manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W01010109 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 105-004509-00
- Product Code / EMDN
- W01010109
- Device Name
- Angiotensin Converting Enzyme Kit (Enzymatic Colorimetric Assay Method)、ACE Calibrator、 ACE Control
- Database Sync Date
- 2026-08-09 16:51:50
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Angiotensin Converting Enzyme (ACE) Kit (Enzymatic Colorimetric Assay Method)?
The registered manufacturer of record for Angiotensin Converting Enzyme (ACE) Kit (Enzymatic Colorimetric Assay Method) is Shenzhen Mindray Bio-Medical Electronics Co., Ltd..
What is the Primary UDI-DI identifier for Angiotensin Converting Enzyme (ACE) Kit (Enzymatic Colorimetric Assay Method)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06944904053363.
What classification code is assigned to this device?
This device is registered under product classification code W01010109.
Similar Classification Devices (W01010109)
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