RevoDx Gastro Pathogen Detection Kit (UDI 08684387210270)
Manufactured by İDİL BİOTECH ARAŞTIRMA SAN. VE TİC. LTD. ŞTİ.
Device Regulatory Overview
The RevoDx Gastro Pathogen Detection Kit (Model/Catalog Number: IP202401-48) is a medical device manufactured by İDİL BİOTECH ARAŞTIRMA SAN. VE TİC. LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification W0105070504 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IP202401-48
- Product Code / EMDN
- W0105070504
- Device Name
- RevoDx Gastro Pathogen Detection Kit
- Database Sync Date
- 2026-08-09 16:49:27
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 RevoDx Gastro Pathogen Detection Kit?
The registered manufacturer of record for RevoDx Gastro Pathogen Detection Kit is İDİL BİOTECH ARAŞTIRMA SAN. VE TİC. LTD. ŞTİ..
What is the Primary UDI-DI identifier for RevoDx Gastro Pathogen Detection Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08684387210270.
What classification code is assigned to this device?
This device is registered under product classification code W0105070504.
Similar Classification Devices (W0105070504)
Other Devices by İDİL BİOTECH ARAŞTIRMA SAN. VE TİC. LTD. ŞTİ.
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