HemosIL Rinse Solution (ACL TOP Family) (UDI 0020302400)
Manufactured by INSTRUMENTATION LABORATORY COMPANY
Device Regulatory Overview
The HemosIL Rinse Solution (ACL TOP Family) (Model/Catalog Number: 0020302400) is a medical device manufactured by INSTRUMENTATION LABORATORY COMPANY. This product is indexed under FDA Product Code / Category Classification JPA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0020302400
- Product Code / EMDN
- JPA
- Device Name
- HemosIL Rinse Solution 4L (ACL TOP Family)
- 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 Rinse Solution (ACL TOP Family)?
The registered manufacturer of record for HemosIL Rinse Solution (ACL TOP Family) is INSTRUMENTATION LABORATORY COMPANY.
What is the Primary UDI-DI identifier for HemosIL Rinse Solution (ACL TOP Family)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0020302400.
What classification code is assigned to this device?
This device is registered under product classification code JPA.
Similar Classification Devices (JPA)
Other Devices by INSTRUMENTATION LABORATORY COMPANY
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