gudid
Primary ID: 2360
Red Dot (UDI 2360)
Manufactured by 3M COMPANY
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Red Dot - Primary ID 2360
Device Regulatory Overview
The Red Dot (Model/Catalog Number: 2360) is a medical device manufactured by 3M COMPANY. This product is indexed under FDA Product Code / Category Classification DRX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2360
- Product Code / EMDN
- DRX
- Device Name
- 3M Red Dot Resting EKG Electrode 2360
- Database Sync Date
- 2026-08-09 09:04:14
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 Red Dot?
The registered manufacturer of record for Red Dot is 3M COMPANY.
What is the Primary UDI-DI identifier for Red Dot?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2360.
What classification code is assigned to this device?
This device is registered under product classification code DRX.
Similar Classification Devices (DRX)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint