eudamed_udi
Primary ID: 17350006444675
CryoIQ Pro Aesthetic Accessories (UDI 17350006444675)
Manufactured by CryoIQ global AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CryoIQ Pro Aesthetic Accessories - Primary ID 17350006444675
Device Regulatory Overview
The CryoIQ Pro Aesthetic Accessories (Model/Catalog Number: CIQ-PSA-C1-7) is a medical device manufactured by CryoIQ global AB. This product is indexed under FDA Product Code / Category Classification Z120102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CIQ-PSA-C1-7
- Product Code / EMDN
- Z120102
- Device Name
- CryoIQ Accessories
- Database Sync Date
- 2026-08-09 16:59:15
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 CryoIQ Pro Aesthetic Accessories?
The registered manufacturer of record for CryoIQ Pro Aesthetic Accessories is CryoIQ global AB.
What is the Primary UDI-DI identifier for CryoIQ Pro Aesthetic Accessories?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 17350006444675.
What classification code is assigned to this device?
This device is registered under product classification code Z120102.
Similar Classification Devices (Z120102)
Other Devices by CryoIQ global AB
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