eudamed_udi
Primary ID: 03661379270523
SET THERAPIE PRESSION NEGATIVE (UDI 03661379270523)
Manufactured by HEMODIA SAS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SET THERAPIE PRESSION NEGATIVE - Primary ID 03661379270523
Device Regulatory Overview
The SET THERAPIE PRESSION NEGATIVE (Model/Catalog Number: 9106_B) is a medical device manufactured by HEMODIA SAS. This product is indexed under FDA Product Code / Category Classification M0499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9106_B
- Product Code / EMDN
- M0499
- Device Name
- Assemblage SUTURE & PLAIES STE
- Database Sync Date
- 2026-08-09 17:02:44
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 SET THERAPIE PRESSION NEGATIVE?
The registered manufacturer of record for SET THERAPIE PRESSION NEGATIVE is HEMODIA SAS.
What is the Primary UDI-DI identifier for SET THERAPIE PRESSION NEGATIVE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03661379270523.
What classification code is assigned to this device?
This device is registered under product classification code M0499.
Similar Classification Devices (M0499)
Other Devices by HEMODIA SAS
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