eudamed_udi
Primary ID: 05701092430946
Scholl Freeze Verruca and Wart Remover (UDI 05701092430946)
Manufactured by CryoConcepts, LP
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Scholl Freeze Verruca and Wart Remover - Primary ID 05701092430946
Device Regulatory Overview
The Scholl Freeze Verruca and Wart Remover (Model/Catalog Number: 1001-0177) is a medical device manufactured by CryoConcepts, LP. This product is indexed under FDA Product Code / Category Classification Z120102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1001-0177
- Product Code / EMDN
- Z120102
- Device Name
- Freeze 'n Clear Skin Clinic Advanced Wart & Verruca Remover
- Database Sync Date
- 2026-08-09 16:59:11
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 Scholl Freeze Verruca and Wart Remover?
The registered manufacturer of record for Scholl Freeze Verruca and Wart Remover is CryoConcepts, LP.
What is the Primary UDI-DI identifier for Scholl Freeze Verruca and Wart Remover?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05701092430946.
What classification code is assigned to this device?
This device is registered under product classification code Z120102.
Similar Classification Devices (Z120102)
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