gudid
Primary ID: 1720WY
Advance Plus Universal IV Administration Set (UDI 1720WY)
Manufactured by Exel International
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Advance Plus Universal IV Administration Set - Primary ID 1720WY
Device Regulatory Overview
The Advance Plus Universal IV Administration Set (Model/Catalog Number: 1720WY) is a medical device manufactured by Exel International. This product is indexed under FDA Product Code / Category Classification FPA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1720WY
- Product Code / EMDN
- FPA
- Device Name
- IV Administration Set, Luer Slip, 1 injection site, 20" tubing
- Database Sync Date
- 2026-08-09 09:00:33
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 Advance Plus Universal IV Administration Set?
The registered manufacturer of record for Advance Plus Universal IV Administration Set is Exel International.
What is the Primary UDI-DI identifier for Advance Plus Universal IV Administration Set?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1720WY.
What classification code is assigned to this device?
This device is registered under product classification code FPA.
Similar Classification Devices (FPA)
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