Alkaline Phosphatase Reagent Kit (UDI D-ALP601AC)
Manufactured by Hangzhou Aichek Medical Technology Co., Ltd.
Device Regulatory Overview
The Alkaline Phosphatase Reagent Kit (Model/Catalog Number: ALP6011Y, ALP6012Y, ALP6013Y, ALP6014Y, ALP6015Y, ALP6011N, ALP6012N, ALP6013N, ALP6014N, ALP6015N) is a medical device manufactured by Hangzhou Aichek Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W01010105 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ALP6011Y, ALP6012Y, ALP6013Y, ALP6014Y, ALP6015Y, ALP6011N, ALP6012N, ALP6013N, ALP6014N, ALP6015N
- Product Code / EMDN
- W01010105
- Device Name
- Alkaline Phosphatase Reagent Kit
- Database Sync Date
- 2026-08-09 16:59:32
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 Alkaline Phosphatase Reagent Kit?
The registered manufacturer of record for Alkaline Phosphatase Reagent Kit is Hangzhou Aichek Medical Technology Co., Ltd..
What is the Primary UDI-DI identifier for Alkaline Phosphatase Reagent Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-ALP601AC.
What classification code is assigned to this device?
This device is registered under product classification code W01010105.
Similar Classification Devices (W01010105)
Other Devices by Hangzhou Aichek Medical Technology Co., Ltd.
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