eudamed_udi
Primary ID: 05055982783224
Skin IQ 365 (UDI 05055982783224)
Manufactured by ArjoHuntleigh AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Skin IQ 365 - Primary ID 05055982783224
Device Regulatory Overview
The Skin IQ 365 (Model/Catalog Number: SIQCPRUS1UN) is a medical device manufactured by ArjoHuntleigh AB. This product is indexed under FDA Product Code / Category Classification Z12019003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SIQCPRUS1UN
- Product Code / EMDN
- Z12019003
- Device Name
- ALPHA ACTIVE 3 PUMP
- Database Sync Date
- 2026-08-09 16:45:44
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 Skin IQ 365?
The registered manufacturer of record for Skin IQ 365 is ArjoHuntleigh AB.
What is the Primary UDI-DI identifier for Skin IQ 365?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05055982783224.
What classification code is assigned to this device?
This device is registered under product classification code Z12019003.
Similar Classification Devices (Z12019003)
Other Devices by ArjoHuntleigh AB
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