GEM Check Coag Control-Abnormal for PT (UDI 06260061700)
Manufactured by INSTRUMENTATION LABORATORY COMPANY
Device Regulatory Overview
The GEM Check Coag Control-Abnormal for PT (Model/Catalog Number: 06260061700) 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
- 06260061700
- Product Code / EMDN
- GGN
- Device Name
- GEM Check Coag Control-Abnormal for PT
- 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 GEM Check Coag Control-Abnormal for PT?
The registered manufacturer of record for GEM Check Coag Control-Abnormal for PT is INSTRUMENTATION LABORATORY COMPANY.
What is the Primary UDI-DI identifier for GEM Check Coag Control-Abnormal for PT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06260061700.
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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