gudid
Primary ID: HW-400-25 P
Surtex (UDI HW-400-25 P)
Manufactured by SURTEX INSTRUMENTS LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Surtex - Primary ID HW-400-25 P
Device Regulatory Overview
The Surtex (Model/Catalog Number: HW-400-25 P) is a medical device manufactured by SURTEX INSTRUMENTS LTD.. This product is indexed under FDA Product Code / Category Classification FSM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HW-400-25 P
- Product Code / EMDN
- FSM
- Device Name
- Kidney Dish Size 250 x 140 x 40 mm Stainless Steel
- Database Sync Date
- 2026-08-09 09:08:11
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 Surtex?
The registered manufacturer of record for Surtex is SURTEX INSTRUMENTS LTD..
What is the Primary UDI-DI identifier for Surtex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HW-400-25 P.
What classification code is assigned to this device?
This device is registered under product classification code FSM.
Similar Classification Devices (FSM)
Other Devices by SURTEX INSTRUMENTS LTD.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint