gudid
Primary ID: IS
HU-FRIEDY (UDI IS)
Manufactured by HU-FRIEDY MFG. CO., LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HU-FRIEDY - Primary ID IS
Device Regulatory Overview
The HU-FRIEDY (Model/Catalog Number: IS) is a medical device manufactured by HU-FRIEDY MFG. CO., LLC. This product is indexed under FDA Product Code / Category Classification EIB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IS
- Product Code / EMDN
- EIB
- Device Name
- Aqua-Fix Irrigating Syringe
- Database Sync Date
- 2026-08-09 09:31:44
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 HU-FRIEDY?
The registered manufacturer of record for HU-FRIEDY is HU-FRIEDY MFG. CO., LLC.
What is the Primary UDI-DI identifier for HU-FRIEDY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is IS.
What classification code is assigned to this device?
This device is registered under product classification code EIB.
Similar Classification Devices (EIB)
Other Devices by HU-FRIEDY MFG. CO., LLC
Programmatic Export
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