GUDIDData
gudid Primary ID: 01-1928

SteriLance Softsense Lancet 28G (UDI 01-1928)

Manufactured by Sterilance Medical (Suzhou) Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SteriLance Softsense Lancet 28G - Primary ID 01-1928

Device Regulatory Overview

The SteriLance Softsense Lancet 28G (Model/Catalog Number: 01-1928) 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
01-1928
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 SteriLance Softsense Lancet 28G?

The registered manufacturer of record for SteriLance Softsense Lancet 28G is Sterilance Medical (Suzhou) Inc..

What is the Primary UDI-DI identifier for SteriLance Softsense Lancet 28G?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 01-1928.

What classification code is assigned to this device?

This device is registered under product classification code QRK.

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