IMMULITE 2000 Systems IGF-I (UDI 11128543)
Manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
Device Regulatory Overview
The IMMULITE 2000 Systems IGF-I (Model/Catalog Number: 11128543) is a medical device manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD. This product is indexed under FDA Product Code / Category Classification CFL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 11128543
- Product Code / EMDN
- CFL
- Device Name
- Insulin-like growth factor I (IGF-I) 200 test kit
- Database Sync Date
- 2026-08-09 09:32:41
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of IMMULITE 2000 Systems IGF-I?
The registered manufacturer of record for IMMULITE 2000 Systems IGF-I is SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD.
What is the Primary UDI-DI identifier for IMMULITE 2000 Systems IGF-I?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 11128543.
What classification code is assigned to this device?
This device is registered under product classification code CFL.
Similar Classification Devices (CFL)
Other Devices by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint