gudid
Primary ID: Quick Connect
NA (UDI Quick Connect)
Manufactured by STERIS CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID Quick Connect
Device Regulatory Overview
The NA (Model/Catalog Number: Quick Connect) is a medical device manufactured by STERIS CORPORATION. This product is indexed under FDA Product Code / Category Classification MED within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Quick Connect
- Product Code / EMDN
- MED
- Device Name
- The Quick Connect for Karl Storz Flexible DCI and Non-Video Anesthesia and ENT Endoscope are used with C1140E Universal Flexible Processing Trays in the System 1 endo Liquid Chemical Processing System.
- Database Sync Date
- 2026-08-09 09:19:08
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 STERIS CORPORATION.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Quick Connect.
What classification code is assigned to this device?
This device is registered under product classification code MED.
Similar Classification Devices (MED)
Other Devices by STERIS CORPORATION
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