F&P FLEXITRUNK (UDI 09420012432469)
Manufactured by Fisher & Paykel Healthcare Limited
Device Regulatory Overview
The F&P FLEXITRUNK (Model/Catalog Number: BC191-05) is a medical device manufactured by Fisher & Paykel Healthcare Limited. This product is indexed under FDA Product Code / Category Classification R02010199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BC191-05
- Product Code / EMDN
- R02010199
- Device Name
- Nasal Tubing 70mm
- Database Sync Date
- 2026-08-09 16:46:10
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 F&P FLEXITRUNK?
The registered manufacturer of record for F&P FLEXITRUNK is Fisher & Paykel Healthcare Limited.
What is the Primary UDI-DI identifier for F&P FLEXITRUNK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09420012432469.
What classification code is assigned to this device?
This device is registered under product classification code R02010199.
Similar Classification Devices (R02010199)
Other Devices by Fisher & Paykel Healthcare Limited
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