BiPAP A40 Pro, Intl w/Heated Tube Humid (UDI 00606959055056)
Manufactured by Respironics Inc.
Device Regulatory Overview
The BiPAP A40 Pro, Intl w/Heated Tube Humid (Model/Catalog Number: INX3100T19) is a medical device manufactured by Respironics Inc.. This product is indexed under FDA Product Code / Category Classification Z12030103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- INX3100T19
- Product Code / EMDN
- Z12030103
- Device Name
- BiPAP A40 Pro, Intl w/Heated Tube Humid
- Database Sync Date
- 2026-08-09 16:29:10
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 BiPAP A40 Pro, Intl w/Heated Tube Humid?
The registered manufacturer of record for BiPAP A40 Pro, Intl w/Heated Tube Humid is Respironics Inc..
What is the Primary UDI-DI identifier for BiPAP A40 Pro, Intl w/Heated Tube Humid?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00606959055056.
What classification code is assigned to this device?
This device is registered under product classification code Z12030103.
Similar Classification Devices (Z12030103)
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