gudid
Primary ID: FREE280
Protech Proguard (UDI FREE280)
Manufactured by EMERSON & CO SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Protech Proguard - Primary ID FREE280
Device Regulatory Overview
The Protech Proguard (Model/Catalog Number: FREE280) is a medical device manufactured by EMERSON & CO SRL. This product is indexed under FDA Product Code / Category Classification KGO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FREE280
- Product Code / EMDN
- KGO
- Device Name
- Radiation Attenuating Surgical Glove
- Database Sync Date
- 2026-08-09 09:04:31
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 Protech Proguard?
The registered manufacturer of record for Protech Proguard is EMERSON & CO SRL.
What is the Primary UDI-DI identifier for Protech Proguard?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FREE280.
What classification code is assigned to this device?
This device is registered under product classification code KGO.
Similar Classification Devices (KGO)
Other Devices by EMERSON & CO SRL
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint