GUDIDData
gudid Primary ID: SHN02GM0123-50

Sterile Blood Lancet (UDI SHN02GM0123-50)

Manufactured by Sterilance Medical (Suzhou) Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sterile Blood Lancet - Primary ID SHN02GM0123-50

Device Regulatory Overview

The Sterile Blood Lancet (Model/Catalog Number: SHN02GM0123-50) is a medical device manufactured by Sterilance Medical (Suzhou) Inc.. This product is indexed under FDA Product Code / Category Classification QRK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SHN02GM0123-50
Product Code / EMDN
QRK
Device Name
Database Sync Date
2026-08-09 09:21:59

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 Sterile Blood Lancet?

The registered manufacturer of record for Sterile Blood Lancet is Sterilance Medical (Suzhou) Inc..

What is the Primary UDI-DI identifier for Sterile Blood Lancet?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SHN02GM0123-50.

What classification code is assigned to this device?

This device is registered under product classification code QRK.

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