GUDIDData
gudid Primary ID: KRP/MYY-M

CRYOPUSH (UDI KRP/MYY-M)

Manufactured by Chengdu Cryo-push Medical Technology Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CRYOPUSH - Primary ID KRP/MYY-M

Device Regulatory Overview

The CRYOPUSH (Model/Catalog Number: KRP/MYY-M) is a medical device manufactured by Chengdu Cryo-push Medical Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification ILO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
KRP/MYY-M
Product Code / EMDN
ILO
Device Name
Pulse Cold Compression Therapy System with Knee cuff
Database Sync Date
2026-08-09 09:06:39

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 CRYOPUSH?

The registered manufacturer of record for CRYOPUSH is Chengdu Cryo-push Medical Technology Co.,Ltd..

What is the Primary UDI-DI identifier for CRYOPUSH?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KRP/MYY-M.

What classification code is assigned to this device?

This device is registered under product classification code ILO.

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