Angiotensin Converting Enzyme (ACE) Test Kit (Colorimetric) (UDI 06971674867852)
Manufactured by Biobase Biodustry(Shandong) Co.,Ltd.
Device Regulatory Overview
The Angiotensin Converting Enzyme (ACE) Test Kit (Colorimetric) (Model/Catalog Number: Calibrator：1mL×1(91132)) is a medical device manufactured by Biobase Biodustry(Shandong) 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
- Calibrator：1mL×1(91132)
- Product Code / EMDN
- W01010109
- Device Name
- Angiotensin Converting Enzyme (ACE) Test Kit (Colorimetric)
- Database Sync Date
- 2026-08-09 18:16:24
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) Test Kit (Colorimetric)?
The registered manufacturer of record for Angiotensin Converting Enzyme (ACE) Test Kit (Colorimetric) is Biobase Biodustry(Shandong) Co.,Ltd..
What is the Primary UDI-DI identifier for Angiotensin Converting Enzyme (ACE) Test Kit (Colorimetric)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06971674867852.
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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