eudamed_udi
Primary ID: 07611600953332
Conviva Hydro+ (UDI 07611600953332)
Manufactured by IVF HARTMANN AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Conviva Hydro+ - Primary ID 07611600953332
Device Regulatory Overview
The Conviva Hydro+ (Model/Catalog Number: 528050) is a medical device manufactured by IVF HARTMANN AG. This product is indexed under FDA Product Code / Category Classification M040204 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 528050
- Product Code / EMDN
- M040204
- Device Name
- DermaPlast Compress Gel
- Database Sync Date
- 2026-08-09 16:47:12
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 Conviva Hydro+?
The registered manufacturer of record for Conviva Hydro+ is IVF HARTMANN AG.
What is the Primary UDI-DI identifier for Conviva Hydro+?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07611600953332.
What classification code is assigned to this device?
This device is registered under product classification code M040204.
Similar Classification Devices (M040204)
Other Devices by IVF HARTMANN AG
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