gudid
Primary ID: SPD12AF01PN1AP
Touch INTL rack (UDI SPD12AF01PN1AP)
Manufactured by Keri Medical SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Touch INTL rack - Primary ID SPD12AF01PN1AP
Device Regulatory Overview
The Touch INTL rack (Model/Catalog Number: SPD12AF01PN1AP) is a medical device manufactured by Keri Medical SA. This product is indexed under FDA Product Code / Category Classification LRP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SPD12AF01PN1AP
- Product Code / EMDN
- LRP
- Device Name
- Database Sync Date
- 2026-08-09 09:16:08
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 Touch INTL rack?
The registered manufacturer of record for Touch INTL rack is Keri Medical SA.
What is the Primary UDI-DI identifier for Touch INTL rack?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SPD12AF01PN1AP.
What classification code is assigned to this device?
This device is registered under product classification code LRP.
Similar Classification Devices (LRP)
Other Devices by Keri Medical SA
Programmatic Export
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