GUDIDData
eudamed_udi Primary ID: 08908021711504

SCARXGEN (UDI 08908021711504)

Manufactured by REGENXGEN BIOSOLUTIONS PRIVATE LIMITED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SCARXGEN - Primary ID 08908021711504

Device Regulatory Overview

The SCARXGEN (Model/Catalog Number: SXG043) is a medical device manufactured by REGENXGEN BIOSOLUTIONS PRIVATE LIMITED. This product is indexed under FDA Product Code / Category Classification M04040701 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SXG043
Product Code / EMDN
M04040701
Device Name
SCARXGEN
Database Sync Date
2026-08-09 16:29:33

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 SCARXGEN?

The registered manufacturer of record for SCARXGEN is REGENXGEN BIOSOLUTIONS PRIVATE LIMITED.

What is the Primary UDI-DI identifier for SCARXGEN?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08908021711504.

What classification code is assigned to this device?

This device is registered under product classification code M04040701.

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