gudid
Primary ID: HC-17
NA (UDI HC-17)
Manufactured by HARITEX CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID HC-17
Device Regulatory Overview
The NA (Model/Catalog Number: HC-17) is a medical device manufactured by HARITEX CORPORATION. This product is indexed under FDA Product Code / Category Classification JOK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HC-17
- Product Code / EMDN
- JOK
- Device Name
- Wire Scissors, Umbilical, Single Use.
- Database Sync Date
- 2026-08-09 09:46:08
Full Regulatory Attributes
🔒 Token Gated
{
"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 NA?
The registered manufacturer of record for NA is HARITEX CORPORATION.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HC-17.
What classification code is assigned to this device?
This device is registered under product classification code JOK.
Similar Classification Devices (JOK)
Other Devices by HARITEX CORPORATION
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