gudid
Primary ID: SD91503812
Surgical Direct (UDI SD91503812)
Manufactured by Surgical Direct, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Surgical Direct - Primary ID SD91503812
Device Regulatory Overview
The Surgical Direct (Model/Catalog Number: SD91503812) is a medical device manufactured by Surgical Direct, Inc.. This product is indexed under FDA Product Code / Category Classification HDF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SD91503812
- Product Code / EMDN
- HDF
- Device Name
- Pederson Vaginal Speculum, Narrow 11.5cm x 1.3cm Blade, For Disposable Smoke Tube, Ebonized
- Database Sync Date
- 2026-08-09 09:00:28
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 Surgical Direct?
The registered manufacturer of record for Surgical Direct is Surgical Direct, Inc..
What is the Primary UDI-DI identifier for Surgical Direct?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SD91503812.
What classification code is assigned to this device?
This device is registered under product classification code HDF.
Similar Classification Devices (HDF)
Other Devices by Surgical Direct, Inc.
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