IMMULITE/IMMULITE 1000 Systems Growth Hormone (UDI 10381433)
Manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
Device Regulatory Overview
The IMMULITE/IMMULITE 1000 Systems Growth Hormone (Model/Catalog Number: 10381433) 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
- 10381433
- Product Code / EMDN
- CFL
- Device Name
- hGH - IMMULITE - RGT - 100 Tests
- Database Sync Date
- 2026-08-09 09:32:40
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 IMMULITE/IMMULITE 1000 Systems Growth Hormone?
The registered manufacturer of record for IMMULITE/IMMULITE 1000 Systems Growth Hormone is SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD.
What is the Primary UDI-DI identifier for IMMULITE/IMMULITE 1000 Systems Growth Hormone?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10381433.
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
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