HemosIL Abnormal Control 2 (UDI 00020014000)
Manufactured by INSTRUMENTATION LABORATORY COMPANY
Device Regulatory Overview
The HemosIL Abnormal Control 2 (Model/Catalog Number: 00020014000) 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
- 00020014000
- Product Code / EMDN
- GGN
- Device Name
- HemosIL Abnormal Control 2
- Database Sync Date
- 2026-08-09 09:10:49
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 Abnormal Control 2?
The registered manufacturer of record for HemosIL Abnormal Control 2 is INSTRUMENTATION LABORATORY COMPANY.
What is the Primary UDI-DI identifier for HemosIL Abnormal Control 2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00020014000.
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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