GUDIDData
eudamed_udi Primary ID: 16926365539485

ScarView (UDI 16926365539485)

Manufactured by Zhejiang Longterm Medical Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ScarView - Primary ID 16926365539485

Device Regulatory Overview

The ScarView (Model/Catalog Number: SCARV30) is a medical device manufactured by Zhejiang Longterm Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification M04040701 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SCARV30
Product Code / EMDN
M04040701
Device Name
silicone gel
Database Sync Date
2026-08-09 16:30:21

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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Frequently Asked Questions

Who is the primary manufacturer of ScarView?

The registered manufacturer of record for ScarView is Zhejiang Longterm Medical Technology Co., Ltd..

What is the Primary UDI-DI identifier for ScarView?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16926365539485.

What classification code is assigned to this device?

This device is registered under product classification code M04040701.

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