eudamed_udi
Primary ID: D-3069AQ
Unspecified Brand (UDI D-3069AQ)
Manufactured by Aikang Diagnostics Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID D-3069AQ
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: AKBR3069030) is a medical device manufactured by Aikang Diagnostics Co., Ltd. This product is indexed under FDA Product Code / Category Classification W0102060103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AKBR3069030
- Product Code / EMDN
- W0102060103
- Device Name
- Insulin in vitro diagnostic kit (Chemiluminescent Immunoassay)
- Database Sync Date
- 2026-08-09 16:45:00
Full Regulatory Attributes
π Token Gated
{
"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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Aikang Diagnostics Co., Ltd.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-3069AQ.
What classification code is assigned to this device?
This device is registered under product classification code W0102060103.
Similar Classification Devices (W0102060103)
Other Devices by Aikang Diagnostics Co., Ltd
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