gudid
Primary ID: SMR352
ECTphan (UDI SMR352)
Manufactured by Providus Holdings, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ECTphan - Primary ID SMR352
Device Regulatory Overview
The ECTphan (Model/Catalog Number: SMR352) is a medical device manufactured by Providus Holdings, Inc.. This product is indexed under FDA Product Code / Category Classification IXF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SMR352
- Product Code / EMDN
- IXF
- Device Name
- Line Source Plugs (Set of 3), Fillable 1mm ID clear urethane rod inset with Luer Lock fittings and end caps.
- Database Sync Date
- 2026-08-09 09:22:08
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 ECTphan?
The registered manufacturer of record for ECTphan is Providus Holdings, Inc..
What is the Primary UDI-DI identifier for ECTphan?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SMR352.
What classification code is assigned to this device?
This device is registered under product classification code IXF.
Similar Classification Devices (IXF)
Other Devices by Providus Holdings, Inc.
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