eudamed_udi
Primary ID: 08033123400190
RETELAST (UDI 08033123400190)
Manufactured by MEDINET SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RETELAST - Primary ID 08033123400190
Device Regulatory Overview
The RETELAST (Model/Catalog Number: 1002025009) is a medical device manufactured by MEDINET SRL. This product is indexed under FDA Product Code / Category Classification M03030103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1002025009
- Product Code / EMDN
- M03030103
- Device Name
- RETELAST
- Database Sync Date
- 2026-08-09 16:29:19
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 RETELAST?
The registered manufacturer of record for RETELAST is MEDINET SRL.
What is the Primary UDI-DI identifier for RETELAST?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033123400190.
What classification code is assigned to this device?
This device is registered under product classification code M03030103.
Similar Classification Devices (M03030103)
Other Devices by MEDINET SRL
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