GUDIDData
eudamed_udi Primary ID: 06974567742335

SCISSORS (UDI 06974567742335)

Manufactured by Wuxi Emsrun Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SCISSORS - Primary ID 06974567742335

Device Regulatory Overview

The SCISSORS (Model/Catalog Number: CR-SC01-7) is a medical device manufactured by Wuxi Emsrun Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification L01040102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CR-SC01-7
Product Code / EMDN
L01040102
Device Name
SCISSORS
Database Sync Date
2026-08-09 16:50:50

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of SCISSORS?

The registered manufacturer of record for SCISSORS is Wuxi Emsrun Technology Co., Ltd..

What is the Primary UDI-DI identifier for SCISSORS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974567742335.

What classification code is assigned to this device?

This device is registered under product classification code L01040102.

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