eudamed_udi
Primary ID: 07395502090004
Unspecified Brand (UDI 07395502090004)
Manufactured by Mediplast AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 07395502090004
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 71100) is a medical device manufactured by Mediplast AB. This product is indexed under FDA Product Code / Category Classification R900902 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 71100
- Product Code / EMDN
- R900902
- Device Name
- Pep/Rmt set with mask
- Database Sync Date
- 2026-08-09 16:48:29
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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Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Mediplast AB.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07395502090004.
What classification code is assigned to this device?
This device is registered under product classification code R900902.
Similar Classification Devices (R900902)
Other Devices by Mediplast AB
Programmatic Export
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