GUDIDData
eudamed_udi Primary ID: 06978920970250

Hot/cold pack gel-zebra (UDI 06978920970250)

Manufactured by Wuhan Pakcare Bio‐technology Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hot/cold pack gel-zebra - Primary ID 06978920970250

Device Regulatory Overview

The Hot/cold pack gel-zebra (Model/Catalog Number: CCKT09) is a medical device manufactured by Wuhan Pakcare Bio‐technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification M9001 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CCKT09
Product Code / EMDN
M9001
Device Name
Reusable Hot/cold packs
Database Sync Date
2026-08-09 16:28:44

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 Hot/cold pack gel-zebra?

The registered manufacturer of record for Hot/cold pack gel-zebra is Wuhan Pakcare Bio‐technology Co.,Ltd..

What is the Primary UDI-DI identifier for Hot/cold pack gel-zebra?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978920970250.

What classification code is assigned to this device?

This device is registered under product classification code M9001.

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