gudid
Primary ID: 33501-23-002
FusionMAX (UDI 33501-23-002)
Manufactured by SURGIX MEDICAL LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FusionMAX - Primary ID 33501-23-002
Device Regulatory Overview
The FusionMAX (Model/Catalog Number: 33501-23-002) is a medical device manufactured by SURGIX MEDICAL LLC. This product is indexed under FDA Product Code / Category Classification JEA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 33501-23-002
- Product Code / EMDN
- JEA
- Device Name
- Supine Table Pad: memory foam cushion designed to be use in conjunction with the Supine Platforms to provide support and comfort to patient in supine position, velcro attachment
- Database Sync Date
- 2026-08-09 09:07:53
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 FusionMAX?
The registered manufacturer of record for FusionMAX is SURGIX MEDICAL LLC.
What is the Primary UDI-DI identifier for FusionMAX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 33501-23-002.
What classification code is assigned to this device?
This device is registered under product classification code JEA.
Similar Classification Devices (JEA)
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