eudamed_udi Primary ID: 06955792736351

Unspecified Brand (UDI 06955792736351)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: S2002E-50) is a medical device manufactured by Sansure Biotech Inc.. This product is indexed under FDA Product Code / Category Classification W0102039001 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: S2002E-50
Product Code / EMDN: W0102039001
Device Name: Alpha-Fetoprotein Chemiluminescence Immunoassay Kit
Database Sync Date: 2026-08-09 16:29:00

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Sansure Biotech Inc..

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06955792736351.

What classification code is assigned to this device?

This device is registered under product classification code W0102039001.

Similar Classification Devices (W0102039001)

Other Devices by Sansure Biotech Inc.

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