gudid
Primary ID: 13325-300
IGF-1 AccuBind ELISA Test System - 96 Wells (UDI 13325-300)
Manufactured by MONOBIND, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IGF-1 AccuBind ELISA Test System - 96 Wells - Primary ID 13325-300
Device Regulatory Overview
The IGF-1 AccuBind ELISA Test System - 96 Wells (Model/Catalog Number: 13325-300) is a medical device manufactured by MONOBIND, INC.. This product is indexed under FDA Product Code / Category Classification CFL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 13325-300
- Product Code / EMDN
- CFL
- Device Name
- Database Sync Date
- 2026-08-09 09:31:26
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 IGF-1 AccuBind ELISA Test System - 96 Wells?
The registered manufacturer of record for IGF-1 AccuBind ELISA Test System - 96 Wells is MONOBIND, INC..
What is the Primary UDI-DI identifier for IGF-1 AccuBind ELISA Test System - 96 Wells?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 13325-300.
What classification code is assigned to this device?
This device is registered under product classification code CFL.
Similar Classification Devices (CFL)
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