gudid
Primary ID: 875
GUM (UDI 875)
Manufactured by SUNSTAR AMERICAS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GUM - Primary ID 875
Device Regulatory Overview
The GUM (Model/Catalog Number: 875) is a medical device manufactured by SUNSTAR AMERICAS, INC.. This product is indexed under FDA Product Code / Category Classification JES within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 875
- Product Code / EMDN
- JES
- Device Name
- GUM Squishmallows KIDS FLOSSERS
- Database Sync Date
- 2026-08-09 09:00:28
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 GUM?
The registered manufacturer of record for GUM is SUNSTAR AMERICAS, INC..
What is the Primary UDI-DI identifier for GUM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 875.
What classification code is assigned to this device?
This device is registered under product classification code JES.
Similar Classification Devices (JES)
Other Devices by SUNSTAR AMERICAS, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint