gudid
Primary ID: 20PS-BL
Litetouch (UDI 20PS-BL)
Manufactured by Asp Global, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Litetouch - Primary ID 20PS-BL
Device Regulatory Overview
The Litetouch (Model/Catalog Number: 20PS-BL) is a medical device manufactured by Asp Global, LLC. This product is indexed under FDA Product Code / Category Classification QRK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20PS-BL
- Product Code / EMDN
- QRK
- Device Name
- LITETOUCH LANCING DEVICE (DOLPHIN) - 1/EA, 1EA/BX, 100BX/IC, 4IC/MCS (400EA)
- Database Sync Date
- 2026-08-09 09:12:13
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 Litetouch?
The registered manufacturer of record for Litetouch is Asp Global, LLC.
What is the Primary UDI-DI identifier for Litetouch?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 20PS-BL.
What classification code is assigned to this device?
This device is registered under product classification code QRK.
Similar Classification Devices (QRK)
Other Devices by Asp Global, LLC
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