eudamed_udi
Primary ID: 08053172971878
C4 (UDI 08053172971878)
Manufactured by GIESSE DIAGNOSTICS SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for C4 - Primary ID 08053172971878
Device Regulatory Overview
The C4 (Model/Catalog Number: 6708) is a medical device manufactured by GIESSE DIAGNOSTICS SRL. This product is indexed under FDA Product Code / Category Classification W0102010205 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6708
- Product Code / EMDN
- W0102010205
- Device Name
- Complemento C4/Complement C4
- Database Sync Date
- 2026-08-09 17:23:21
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 C4?
The registered manufacturer of record for C4 is GIESSE DIAGNOSTICS SRL.
What is the Primary UDI-DI identifier for C4?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053172971878.
What classification code is assigned to this device?
This device is registered under product classification code W0102010205.
Similar Classification Devices (W0102010205)
Other Devices by GIESSE DIAGNOSTICS SRL
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