Angiotensin Converting Enzyme Kit (Kinetic Method with FAPGG) (UDI 06936595751864)
Manufactured by MedicalSystem Biotechnology Co., Ltd.
Device Regulatory Overview
The Angiotensin Converting Enzyme Kit (Kinetic Method with FAPGG) (Model/Catalog Number: Angiotensin Converting Enzyme Kit (Kinetic Method with FAPGG)) is a medical device manufactured by MedicalSystem Biotechnology 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
- Angiotensin Converting Enzyme Kit (Kinetic Method with FAPGG)
- Product Code / EMDN
- W01010109
- Device Name
- Angiotensin Converting Enzyme Kit (Kinetic Method with FAPGG)
- Database Sync Date
- 2026-08-09 19:06:13
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 Kit (Kinetic Method with FAPGG)?
The registered manufacturer of record for Angiotensin Converting Enzyme Kit (Kinetic Method with FAPGG) is MedicalSystem Biotechnology Co., Ltd..
What is the Primary UDI-DI identifier for Angiotensin Converting Enzyme Kit (Kinetic Method with FAPGG)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06936595751864.
What classification code is assigned to this device?
This device is registered under product classification code W01010109.
Similar Classification Devices (W01010109)
Other Devices by MedicalSystem Biotechnology Co., Ltd.
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