gudid
Primary ID: SleeveS
Protech Proguard (UDI SleeveS)
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 SleeveS
Device Regulatory Overview
The Protech Proguard (Model/Catalog Number: SleeveS) is a medical device manufactured by EMERSON & CO SRL. This product is indexed under FDA Product Code / Category Classification KPY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SleeveS
- Product Code / EMDN
- KPY
- Device Name
- Radiation Reducing Sleeves
- 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 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 SleeveS.
What classification code is assigned to this device?
This device is registered under product classification code KPY.
Similar Classification Devices (KPY)
Other Devices by EMERSON & CO SRL
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