GUDIDData
eudamed_udi Primary ID: 08681285109200

Getwell (UDI 08681285109200)

Manufactured by Honnes Sağlık ve Endüstriyel Ürünleri A.Ş

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Getwell - Primary ID 08681285109200

Device Regulatory Overview

The Getwell (Model/Catalog Number: G1011) is a medical device manufactured by Honnes Sağlık ve Endüstriyel Ürünleri A.Ş. This product is indexed under FDA Product Code / Category Classification M04040502 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
G1011
Product Code / EMDN
M04040502
Device Name
COOLING FEVER PATCH
Database Sync Date
2026-08-09 16:30:07

Full Regulatory Attributes

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Getwell?

The registered manufacturer of record for Getwell is Honnes Sağlık ve Endüstriyel Ürünleri A.Ş.

What is the Primary UDI-DI identifier for Getwell?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681285109200.

What classification code is assigned to this device?

This device is registered under product classification code M04040502.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint