gudid
Primary ID: 11006802080F1
Front1 Health Partners (UDI 11006802080F1)
Manufactured by DEGANIA SILICONE LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Front1 Health Partners - Primary ID 11006802080F1
Device Regulatory Overview
The Front1 Health Partners (Model/Catalog Number: 11006802080F1) is a medical device manufactured by DEGANIA SILICONE LTD. This product is indexed under FDA Product Code / Category Classification GBS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 11006802080F1
- Product Code / EMDN
- GBS
- Device Name
- Straight silicone wound drain 20Fr
- Database Sync Date
- 2026-08-09 09:18:12
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 Front1 Health Partners?
The registered manufacturer of record for Front1 Health Partners is DEGANIA SILICONE LTD.
What is the Primary UDI-DI identifier for Front1 Health Partners?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 11006802080F1.
What classification code is assigned to this device?
This device is registered under product classification code GBS.
Similar Classification Devices (GBS)
Other Devices by DEGANIA SILICONE LTD
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