Pressure Monitoring Line with Nafion Dryer (BioMed Private Label) (UDI R229P18-001)
Manufactured by MAXTEC, LLC
Device Regulatory Overview
The Pressure Monitoring Line with Nafion Dryer (BioMed Private Label) (Model/Catalog Number: R229P18-001) is a medical device manufactured by MAXTEC, LLC. This product is indexed under FDA Product Code / Category Classification CBQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R229P18-001
- Product Code / EMDN
- CBQ
- Device Name
- Pressure Monitoring Line with Nafion Dryer (BioMed Private Label) - SINGLE, EACHES LEVEL
- Database Sync Date
- 2026-08-09 09:32:57
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 Pressure Monitoring Line with Nafion Dryer (BioMed Private Label)?
The registered manufacturer of record for Pressure Monitoring Line with Nafion Dryer (BioMed Private Label) is MAXTEC, LLC.
What is the Primary UDI-DI identifier for Pressure Monitoring Line with Nafion Dryer (BioMed Private Label)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is R229P18-001.
What classification code is assigned to this device?
This device is registered under product classification code CBQ.
Similar Classification Devices (CBQ)
Other Devices by MAXTEC, LLC
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