HemosIL CL Rinse solution (UDI 0029781038)
Manufactured by INSTRUMENTATION LABORATORY COMPANY
Device Regulatory Overview
The HemosIL CL Rinse solution (Model/Catalog Number: 0029781038) 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
- 0029781038
- Product Code / EMDN
- JPA
- Device Name
- HemosIL CL Rinse solution
- 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 CL Rinse solution?
The registered manufacturer of record for HemosIL CL Rinse solution is INSTRUMENTATION LABORATORY COMPANY.
What is the Primary UDI-DI identifier for HemosIL CL Rinse solution?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0029781038.
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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