gudid
Primary ID: HMIX4.21 RFID version (white/red shell)
HemoMix 4 (UDI HMIX4.21 RFID version (white/red shell))
Manufactured by DELCON SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HemoMix 4 - Primary ID HMIX4.21 RFID version (white/red shell)
Device Regulatory Overview
The HemoMix 4 (Model/Catalog Number: HMIX4.21 RFID version (white/red shell)) is a medical device manufactured by DELCON SRL. This product is indexed under FDA Product Code / Category Classification MYJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HMIX4.21 RFID version (white/red shell)
- Product Code / EMDN
- MYJ
- Device Name
- HemoMix 4 is an automated blood monitor/mixer used during blood donation to mix the anti-coagulant contained in the blood bag with the whole blood collected during donation and automatically clamping the tube when the target volume has been reached
- Database Sync Date
- 2026-08-09 09:04:33
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 HemoMix 4?
The registered manufacturer of record for HemoMix 4 is DELCON SRL.
What is the Primary UDI-DI identifier for HemoMix 4?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HMIX4.21 RFID version (white/red shell).
What classification code is assigned to this device?
This device is registered under product classification code MYJ.
Similar Classification Devices (MYJ)
Other Devices by DELCON SRL
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