eudamed_udi
Primary ID: 08058090049012
AIRCube2 (UDI 08058090049012)
Manufactured by Pikdare S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AIRCube2 - Primary ID 08058090049012
Device Regulatory Overview
The AIRCube2 (Model/Catalog Number: 58038220000500) is a medical device manufactured by Pikdare S.p.A.. This product is indexed under FDA Product Code / Category Classification Z12159002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 58038220000500
- Product Code / EMDN
- Z12159002
- Device Name
- AIRCube2
- Database Sync Date
- 2026-08-09 16:44:55
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 AIRCube2?
The registered manufacturer of record for AIRCube2 is Pikdare S.p.A..
What is the Primary UDI-DI identifier for AIRCube2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058090049012.
What classification code is assigned to this device?
This device is registered under product classification code Z12159002.
Similar Classification Devices (Z12159002)
Other Devices by Pikdare S.p.A.
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