eudamed_udi
Primary ID: 16438153819322
Complement C4 (UDI 16438153819322)
Manufactured by Thermo Fisher Scientific Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Complement C4 - Primary ID 16438153819322
Device Regulatory Overview
The Complement C4 (Model/Catalog Number: 981932) is a medical device manufactured by Thermo Fisher Scientific Oy. This product is indexed under FDA Product Code / Category Classification W0102010205 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 981932
- Product Code / EMDN
- W0102010205
- Device Name
- Complement C4
- Database Sync Date
- 2026-08-09 16:44:57
Full Regulatory Attributes
๐ 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 Complement C4?
The registered manufacturer of record for Complement C4 is Thermo Fisher Scientific Oy.
What is the Primary UDI-DI identifier for Complement C4?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16438153819322.
What classification code is assigned to this device?
This device is registered under product classification code W0102010205.
Similar Classification Devices (W0102010205)
Other Devices by Thermo Fisher Scientific Oy
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint