eudamed_udi
Primary ID: 04046678003376
Pluto (UDI 04046678003376)
Manufactured by REBOTEC Rehabilitationsmittel GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pluto - Primary ID 04046678003376
Device Regulatory Overview
The Pluto (Model/Catalog Number: 1870020) is a medical device manufactured by REBOTEC Rehabilitationsmittel GmbH. This product is indexed under FDA Product Code / Category Classification Y120606 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1870020
- Product Code / EMDN
- Y120606
- Device Name
- Lauflernhilfen
- Database Sync Date
- 2026-08-09 16:47:04
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 Pluto?
The registered manufacturer of record for Pluto is REBOTEC Rehabilitationsmittel GmbH.
What is the Primary UDI-DI identifier for Pluto?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04046678003376.
What classification code is assigned to this device?
This device is registered under product classification code Y120606.
Similar Classification Devices (Y120606)
Other Devices by REBOTEC Rehabilitationsmittel GmbH
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