gudid
Primary ID: CIQ-P-L/D2
CryoIQ PRO liquid D2 (UDI CIQ-P-L/D2)
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 liquid D2 - Primary ID CIQ-P-L/D2
Device Regulatory Overview
The CryoIQ PRO liquid D2 (Model/Catalog Number: CIQ-P-L/D2) is a medical device manufactured by CryoIQ global AB. This product is indexed under FDA Product Code / Category Classification GEH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CIQ-P-L/D2
- Product Code / EMDN
- GEH
- Device Name
- CryoIQ PRO liquid/Derm 2
- Database Sync Date
- 2026-08-09 09:48:57
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 liquid D2?
The registered manufacturer of record for CryoIQ PRO liquid D2 is CryoIQ global AB.
What is the Primary UDI-DI identifier for CryoIQ PRO liquid D2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CIQ-P-L/D2.
What classification code is assigned to this device?
This device is registered under product classification code GEH.
Similar Classification Devices (GEH)
Other Devices by CryoIQ global AB
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