gudid
Primary ID: S09
Spandage (UDI S09)
Manufactured by MEDI-TECH INTERNATIONAL CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Spandage - Primary ID S09
Device Regulatory Overview
The Spandage (Model/Catalog Number: S09) is a medical device manufactured by MEDI-TECH INTERNATIONAL CORPORATION. This product is indexed under FDA Product Code / Category Classification FQM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S09
- Product Code / EMDN
- FQM
- Device Name
- Original Spandage Tubular Elastic Retainer Net - Size 9 - 25 Yds (stretched)
- Database Sync Date
- 2026-08-09 09:00:32
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 Spandage?
The registered manufacturer of record for Spandage is MEDI-TECH INTERNATIONAL CORPORATION.
What is the Primary UDI-DI identifier for Spandage?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S09.
What classification code is assigned to this device?
This device is registered under product classification code FQM.
Similar Classification Devices (FQM)
Other Devices by MEDI-TECH INTERNATIONAL CORPORATION
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