gudid
Primary ID: LISTER SCISSORS
SCISSORS (UDI LISTER SCISSORS)
Manufactured by DR.FRIGZ INTERNATIONAL(PVT)LTD,
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SCISSORS - Primary ID LISTER SCISSORS
Device Regulatory Overview
The SCISSORS (Model/Catalog Number: LISTER SCISSORS) is a medical device manufactured by DR.FRIGZ INTERNATIONAL(PVT)LTD,. This product is indexed under FDA Product Code / Category Classification JOK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LISTER SCISSORS
- Product Code / EMDN
- JOK
- Device Name
- LISTER SCISSORS ANGLED 5-1/2"
- Database Sync Date
- 2026-08-09 09:06:20
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 SCISSORS?
The registered manufacturer of record for SCISSORS is DR.FRIGZ INTERNATIONAL(PVT)LTD,.
What is the Primary UDI-DI identifier for SCISSORS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LISTER SCISSORS.
What classification code is assigned to this device?
This device is registered under product classification code JOK.
Similar Classification Devices (JOK)
Other Devices by DR.FRIGZ INTERNATIONAL(PVT)LTD,
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