eudamed_udi
Primary ID: 07611600994328
DermaPlast plaster case (UDI 07611600994328)
Manufactured by IVF HARTMANN AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DermaPlast plaster case - Primary ID 07611600994328
Device Regulatory Overview
The DermaPlast plaster case (Model/Catalog Number: 500027) is a medical device manufactured by IVF HARTMANN AG. This product is indexed under FDA Product Code / Category Classification M04010199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 500027
- Product Code / EMDN
- M04010199
- Device Name
- Plaster Sheaths
- Database Sync Date
- 2026-08-09 16:48:36
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 DermaPlast plaster case?
The registered manufacturer of record for DermaPlast plaster case is IVF HARTMANN AG.
What is the Primary UDI-DI identifier for DermaPlast plaster case?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07611600994328.
What classification code is assigned to this device?
This device is registered under product classification code M04010199.
Similar Classification Devices (M04010199)
Other Devices by IVF HARTMANN AG
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