eudamed_udi
Primary ID: 00840363365848
Lateral Pad (UDI 00840363365848)
Manufactured by Ki Mobility LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lateral Pad - Primary ID 00840363365848
Device Regulatory Overview
The Lateral Pad (Model/Catalog Number: PBLAS4X5PR) is a medical device manufactured by Ki Mobility LLC. This product is indexed under FDA Product Code / Category Classification Y122499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PBLAS4X5PR
- Product Code / EMDN
- Y122499
- Device Name
- Backs
- Database Sync Date
- 2026-08-09 16:28:59
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 Lateral Pad?
The registered manufacturer of record for Lateral Pad is Ki Mobility LLC.
What is the Primary UDI-DI identifier for Lateral Pad?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840363365848.
What classification code is assigned to this device?
This device is registered under product classification code Y122499.
Similar Classification Devices (Y122499)
Other Devices by Ki Mobility LLC
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