gudid
Primary ID: 936703F
RADIOLUCENT ARMBOARD WITH 2 INCH POLYFOAM PAD (UDI 936703F)
Manufactured by ALIMED, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RADIOLUCENT ARMBOARD WITH 2 INCH POLYFOAM PAD - Primary ID 936703F
Device Regulatory Overview
The RADIOLUCENT ARMBOARD WITH 2 INCH POLYFOAM PAD (Model/Catalog Number: 936703F) is a medical device manufactured by ALIMED, INC.. This product is indexed under FDA Product Code / Category Classification FWZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 936703F
- Product Code / EMDN
- FWZ
- Device Name
- Database Sync Date
- 2026-08-09 09:54:33
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 RADIOLUCENT ARMBOARD WITH 2 INCH POLYFOAM PAD?
The registered manufacturer of record for RADIOLUCENT ARMBOARD WITH 2 INCH POLYFOAM PAD is ALIMED, INC..
What is the Primary UDI-DI identifier for RADIOLUCENT ARMBOARD WITH 2 INCH POLYFOAM PAD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 936703F.
What classification code is assigned to this device?
This device is registered under product classification code FWZ.
Similar Classification Devices (FWZ)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint