Acido Urico - Biotecnica Systems (UDI 08053172972844)
Manufactured by GIESSE DIAGNOSTICS SRL
Device Regulatory Overview
The Acido Urico - Biotecnica Systems (Model/Catalog Number: BT4050) is a medical device manufactured by GIESSE DIAGNOSTICS SRL. This product is indexed under FDA Product Code / Category Classification W01010232 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BT4050
- Product Code / EMDN
- W01010232
- Device Name
- Acido Urico/Uric Acid - Biotecnica Systems
- Database Sync Date
- 2026-08-09 16:29:10
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 Acido Urico - Biotecnica Systems?
The registered manufacturer of record for Acido Urico - Biotecnica Systems is GIESSE DIAGNOSTICS SRL.
What is the Primary UDI-DI identifier for Acido Urico - Biotecnica Systems?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053172972844.
What classification code is assigned to this device?
This device is registered under product classification code W01010232.
Similar Classification Devices (W01010232)
Other Devices by GIESSE DIAGNOSTICS SRL
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