gudid
Primary ID: WIRE CUTTER SCISSORS
SCISSORS (UDI WIRE CUTTER 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 WIRE CUTTER SCISSORS
Device Regulatory Overview
The SCISSORS (Model/Catalog Number: WIRE CUTTER 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
- WIRE CUTTER SCISSORS
- Product Code / EMDN
- JOK
- Device Name
- WIRE CUTTER SCISSORS 4-3/4"
- 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 WIRE CUTTER 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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