gudid
Primary ID: GY-233-04
Surtex (UDI GY-233-04)
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 GY-233-04
Device Regulatory Overview
The Surtex (Model/Catalog Number: GY-233-04) is a medical device manufactured by SURTEX INSTRUMENTS LTD.. This product is indexed under FDA Product Code / Category Classification HDF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GY-233-04
- Product Code / EMDN
- HDF
- Device Name
- Doyen Vaginal Speculum Slightly Concave-Fig. 4 Blade Size 160 x 47 mm Stainless Steel
- Database Sync Date
- 2026-08-09 09:08:20
Full Regulatory Attributes
🔒 Token Gated
{
"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 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 GY-233-04.
What classification code is assigned to this device?
This device is registered under product classification code HDF.
Similar Classification Devices (HDF)
Other Devices by SURTEX INSTRUMENTS LTD.
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