HemosIL Low Abnormal Control ASSAYED (UDI 00020003210)
Manufactured by INSTRUMENTATION LABORATORY COMPANY
Device Regulatory Overview
The HemosIL Low Abnormal Control ASSAYED (Model/Catalog Number: 00020003210) is a medical device manufactured by INSTRUMENTATION LABORATORY COMPANY. This product is indexed under FDA Product Code / Category Classification GGN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 00020003210
- Product Code / EMDN
- GGN
- Device Name
- HemosIL Low Abnormal Control ASSAYED
- Database Sync Date
- 2026-08-09 09:10:50
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 HemosIL Low Abnormal Control ASSAYED?
The registered manufacturer of record for HemosIL Low Abnormal Control ASSAYED is INSTRUMENTATION LABORATORY COMPANY.
What is the Primary UDI-DI identifier for HemosIL Low Abnormal Control ASSAYED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00020003210.
What classification code is assigned to this device?
This device is registered under product classification code GGN.
Similar Classification Devices (GGN)
Other Devices by INSTRUMENTATION LABORATORY COMPANY
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