eudamed_udi
Primary ID: 08053307590950
EXAIRO PLUS (UDI 08053307590950)
Manufactured by Technix S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EXAIRO PLUS - Primary ID 08053307590950
Device Regulatory Overview
The EXAIRO PLUS (Model/Catalog Number: EXAIRO-P) is a medical device manufactured by Technix S.p.A.. This product is indexed under FDA Product Code / Category Classification Z11039016 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EXAIRO-P
- Product Code / EMDN
- Z11039016
- Device Name
- Mobile radiologic units
- Database Sync Date
- 2026-08-09 17:17:10
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 EXAIRO PLUS?
The registered manufacturer of record for EXAIRO PLUS is Technix S.p.A..
What is the Primary UDI-DI identifier for EXAIRO PLUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053307590950.
What classification code is assigned to this device?
This device is registered under product classification code Z11039016.
Similar Classification Devices (Z11039016)
Other Devices by Technix S.p.A.
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