gudid
Primary ID: IPN049318
HUDSON RCI (UDI IPN049318)
Manufactured by TELEFLEX INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HUDSON RCI - Primary ID IPN049318
Device Regulatory Overview
The HUDSON RCI (Model/Catalog Number: IPN049318) is a medical device manufactured by TELEFLEX INCORPORATED. This product is indexed under FDA Product Code / Category Classification BWF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IPN049318
- Product Code / EMDN
- BWF
- Device Name
- VOLUMETRIC EXERCISER For Maintaining and Improving Inspiratory Volume and Respiratory Fitness
- Database Sync Date
- 2026-08-09 09:48:32
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of HUDSON RCI?
The registered manufacturer of record for HUDSON RCI is TELEFLEX INCORPORATED.
What is the Primary UDI-DI identifier for HUDSON RCI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is IPN049318.
What classification code is assigned to this device?
This device is registered under product classification code BWF.
Similar Classification Devices (BWF)
Other Devices by TELEFLEX INCORPORATED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint