gudid
Primary ID: Bolx II
Action (UDI Bolx II)
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 Bolx II
Device Regulatory Overview
The Action (Model/Catalog Number: Bolx II) is a medical device manufactured by ACTION PRODUCTS, INC.. This product is indexed under FDA Product Code / Category Classification JAD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Bolx II
- Product Code / EMDN
- JAD
- Device Name
- Database Sync Date
- 2026-08-09 09:08:43
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 Bolx II.
What classification code is assigned to this device?
This device is registered under product classification code JAD.
Similar Classification Devices (JAD)
Other Devices by ACTION PRODUCTS, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint