eudamed_udi
Primary ID: 16945630139380
SteriLance (UDI 16945630139380)
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 - Primary ID 16945630139380
Device Regulatory Overview
The SteriLance (Model/Catalog Number: Soft 30G) is a medical device manufactured by Sterilance Medical (Suzhou) Inc.. This product is indexed under FDA Product Code / Category Classification V010402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Soft 30G
- Product Code / EMDN
- V010402
- Device Name
- Disposable Blood Lancets
- Database Sync Date
- 2026-08-09 16:46:27
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of SteriLance?
The registered manufacturer of record for SteriLance is Sterilance Medical (Suzhou) Inc..
What is the Primary UDI-DI identifier for SteriLance?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16945630139380.
What classification code is assigned to this device?
This device is registered under product classification code V010402.
Similar Classification Devices (V010402)
Other Devices by Sterilance Medical (Suzhou) Inc.
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