gudid
Primary ID: A2003
Amazfit (UDI A2003)
Manufactured by Anhui Huami Healthcare Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Amazfit - Primary ID A2003
Device Regulatory Overview
The Amazfit (Model/Catalog Number: A2003) is a medical device manufactured by Anhui Huami Healthcare Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification PUH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A2003
- Product Code / EMDN
- PUH
- Device Name
- Database Sync Date
- 2026-08-09 09:06:41
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 Amazfit?
The registered manufacturer of record for Amazfit is Anhui Huami Healthcare Co.,Ltd..
What is the Primary UDI-DI identifier for Amazfit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A2003.
What classification code is assigned to this device?
This device is registered under product classification code PUH.
Similar Classification Devices (PUH)
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