IDS-iSYS 17-OH Progesterone (UDI 05060169690738)
Manufactured by Immunodiagnostic Systems Limited
Device Regulatory Overview
The IDS-iSYS 17-OH Progesterone (Model/Catalog Number: IS-5100) is a medical device manufactured by Immunodiagnostic Systems Limited. This product is indexed under FDA Product Code / Category Classification W0102050106 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IS-5100
- Product Code / EMDN
- W0102050106
- Device Name
- IDS-iSYS 17-OH Progesterone
- Database Sync Date
- 2026-08-09 17:09:57
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 IDS-iSYS 17-OH Progesterone?
The registered manufacturer of record for IDS-iSYS 17-OH Progesterone is Immunodiagnostic Systems Limited.
What is the Primary UDI-DI identifier for IDS-iSYS 17-OH Progesterone?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060169690738.
What classification code is assigned to this device?
This device is registered under product classification code W0102050106.
Similar Classification Devices (W0102050106)
Other Devices by Immunodiagnostic Systems Limited
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint