gudid
Primary ID: SMCLIPPER
SourceMark (UDI SMCLIPPER)
Manufactured by SOURCEMARK, LLC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SourceMark - Primary ID SMCLIPPER
Device Regulatory Overview
The SourceMark (Model/Catalog Number: SMCLIPPER) is a medical device manufactured by SOURCEMARK, LLC.. This product is indexed under FDA Product Code / Category Classification LWK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SMCLIPPER
- Product Code / EMDN
- LWK
- Device Name
- Database Sync Date
- 2026-08-09 09:43:34
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 SourceMark?
The registered manufacturer of record for SourceMark is SOURCEMARK, LLC..
What is the Primary UDI-DI identifier for SourceMark?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SMCLIPPER.
What classification code is assigned to this device?
This device is registered under product classification code LWK.
Similar Classification Devices (LWK)
Other Devices by SOURCEMARK, LLC.
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