gudid
Primary ID: Model170
Freeguard (UDI Model170)
Manufactured by EMERSON & CO SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Freeguard - Primary ID Model170
Device Regulatory Overview
The Freeguard (Model/Catalog Number: Model170) 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
- Model170
- Product Code / EMDN
- KGO
- Device Name
- Radiation Attenuating Surgical Glove
- Database Sync Date
- 2026-08-09 09:04:31
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Freeguard?
The registered manufacturer of record for Freeguard is EMERSON & CO SRL.
What is the Primary UDI-DI identifier for Freeguard?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Model170.
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
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JSON API Endpoint