gudid
Primary ID: Adaptive Pad
Action (UDI Adaptive Pad)
Manufactured by ACTION PRODUCTS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Action - Primary ID Adaptive Pad
Device Regulatory Overview
The Action (Model/Catalog Number: Adaptive Pad) is a medical device manufactured by ACTION PRODUCTS, INC.. This product is indexed under FDA Product Code / Category Classification KIC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Adaptive Pad
- Product Code / EMDN
- KIC
- Device Name
- Action Adaptive Cube Pad
- Database Sync Date
- 2026-08-09 09:08:43
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 Action?
The registered manufacturer of record for Action is ACTION PRODUCTS, INC..
What is the Primary UDI-DI identifier for Action?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Adaptive Pad.
What classification code is assigned to this device?
This device is registered under product classification code KIC.
Similar Classification Devices (KIC)
Other Devices by ACTION PRODUCTS, INC.
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