HGH CLIA Microparticles (UDI 06970150908911)
Manufactured by Autobio Diagnostics Co., Ltd.
Device Regulatory Overview
The HGH CLIA Microparticles (Model/Catalog Number: CML0202) is a medical device manufactured by Autobio Diagnostics Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102060402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CML0202
- Product Code / EMDN
- W0102060402
- Device Name
- AutoLumo Analyzer
- Database Sync Date
- 2026-08-09 16:29:15
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 HGH CLIA Microparticles?
The registered manufacturer of record for HGH CLIA Microparticles is Autobio Diagnostics Co., Ltd..
What is the Primary UDI-DI identifier for HGH CLIA Microparticles?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970150908911.
What classification code is assigned to this device?
This device is registered under product classification code W0102060402.
Similar Classification Devices (W0102060402)
Other Devices by Autobio Diagnostics Co., Ltd.
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