Valve anti-retour expiration blanche 22M-22F (UDI 03666256010889)
Manufactured by Int'Air Médical
Device Regulatory Overview
The Valve anti-retour expiration blanche 22M-22F (Model/Catalog Number: AC11.WW) is a medical device manufactured by Int'Air Médical. This product is indexed under FDA Product Code / Category Classification R028001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AC11.WW
- Product Code / EMDN
- R028001
- Device Name
- Accessoires de circuits de ventilation non stériles
- Database Sync Date
- 2026-08-09 18:08:49
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 Valve anti-retour expiration blanche 22M-22F?
The registered manufacturer of record for Valve anti-retour expiration blanche 22M-22F is Int'Air Médical.
What is the Primary UDI-DI identifier for Valve anti-retour expiration blanche 22M-22F?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03666256010889.
What classification code is assigned to this device?
This device is registered under product classification code R028001.
Similar Classification Devices (R028001)
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