GUDIDData
eudamed_udi Primary ID: 06978920973206

MULTI PURPOSE GEL PACK, MEDIUM SIZE (UDI 06978920973206)

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 MULTI PURPOSE GEL PACK, MEDIUM SIZE - Primary ID 06978920973206

Device Regulatory Overview

The MULTI PURPOSE GEL PACK, MEDIUM SIZE (Model/Catalog Number: AGFX63) 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
AGFX63
Product Code / EMDN
M9001
Device Name
Reusable Hot/cold packs
Database Sync Date
2026-08-09 16:28:46

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 MULTI PURPOSE GEL PACK, MEDIUM SIZE?

The registered manufacturer of record for MULTI PURPOSE GEL PACK, MEDIUM SIZE is Wuhan Pakcare Bio‐technology Co.,Ltd..

What is the Primary UDI-DI identifier for MULTI PURPOSE GEL PACK, MEDIUM SIZE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978920973206.

What classification code is assigned to this device?

This device is registered under product classification code M9001.

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