gudid
Primary ID: 201TC
Litetouch (UDI 201TC)
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 201TC
Device Regulatory Overview
The Litetouch (Model/Catalog Number: 201TC) 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
- 201TC
- Product Code / EMDN
- QRK
- Device Name
- LITE TOUCH ULTRA THIN LANCETS - 30G - 1/EA, 100EA/BX, 100BX/CS (10000EA)
- 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 201TC.
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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