eudamed_udi
Primary ID: 05413765581816
EVO IQ (UDI 05413765581816)
Manufactured by Baxter Healthcare SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EVO IQ - Primary ID 05413765581816
Device Regulatory Overview
The EVO IQ (Model/Catalog Number: ESYR001GRC) is a medical device manufactured by Baxter Healthcare SA. This product is indexed under FDA Product Code / Category Classification Z12030302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ESYR001GRC
- Product Code / EMDN
- Z12030302
- Device Name
- Evo IQ Syringe Infusion Pump
- Database Sync Date
- 2026-08-09 16:30:07
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 EVO IQ?
The registered manufacturer of record for EVO IQ is Baxter Healthcare SA.
What is the Primary UDI-DI identifier for EVO IQ?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05413765581816.
What classification code is assigned to this device?
This device is registered under product classification code Z12030302.
Similar Classification Devices (Z12030302)
Other Devices by Baxter Healthcare SA
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