GUDIDData
gudid Primary ID: CIQ-PA-D1

CryoIQ Dermatology tip D1 (UDI CIQ-PA-D1)

Manufactured by CryoIQ global AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CryoIQ Dermatology tip D1 - Primary ID CIQ-PA-D1

Device Regulatory Overview

The CryoIQ Dermatology tip D1 (Model/Catalog Number: CIQ-PA-D1) 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-PA-D1
Product Code / EMDN
GEH
Device Name
Dermatology tip, L=22 mm, spray freezing 1-6 mm for PRO
Database Sync Date
2026-08-09 09:48:57

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of CryoIQ Dermatology tip D1?

The registered manufacturer of record for CryoIQ Dermatology tip D1 is CryoIQ global AB.

What is the Primary UDI-DI identifier for CryoIQ Dermatology tip D1?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CIQ-PA-D1.

What classification code is assigned to this device?

This device is registered under product classification code GEH.

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