eudamed_udi
Primary ID: 00606959001794
S FITLIFE MASK EE W/HGR INT (UDI 00606959001794)
Manufactured by Respironics Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for S FITLIFE MASK EE W/HGR INT - Primary ID 00606959001794
Device Regulatory Overview
The S FITLIFE MASK EE W/HGR INT (Model/Catalog Number: 1060803) is a medical device manufactured by Respironics Inc.. This product is indexed under FDA Product Code / Category Classification R0301010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1060803
- Product Code / EMDN
- R0301010202
- Device Name
- FitLife Family
- Database Sync Date
- 2026-08-09 16:29:22
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 S FITLIFE MASK EE W/HGR INT?
The registered manufacturer of record for S FITLIFE MASK EE W/HGR INT is Respironics Inc..
What is the Primary UDI-DI identifier for S FITLIFE MASK EE W/HGR INT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00606959001794.
What classification code is assigned to this device?
This device is registered under product classification code R0301010202.
Similar Classification Devices (R0301010202)
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