Myoglobin Test (UDI 06958982140907)
Manufactured by Abiores Technology (Beijing) Co.,Ltd.
Device Regulatory Overview
The Myoglobin Test (Model/Catalog Number: ACA21B002-001D) is a medical device manufactured by Abiores Technology (Beijing) Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160702 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ACA21B002-001D
- Product Code / EMDN
- W0102160702
- Device Name
- Myoglobin Test
- Database Sync Date
- 2026-08-09 17:13:15
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 Myoglobin Test?
The registered manufacturer of record for Myoglobin Test is Abiores Technology (Beijing) Co.,Ltd..
What is the Primary UDI-DI identifier for Myoglobin Test?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06958982140907.
What classification code is assigned to this device?
This device is registered under product classification code W0102160702.
Similar Classification Devices (W0102160702)
Other Devices by Abiores Technology (Beijing) Co.,Ltd.
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