eudamed_udi
Primary ID: 05414874020869
Sensilind Complete Care From maxi 8 (UDI 05414874020869)
Manufactured by Ontex BV
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sensilind Complete Care From maxi 8 - Primary ID 05414874020869
Device Regulatory Overview
The Sensilind Complete Care From maxi 8 (Model/Catalog Number: 12.08.1) is a medical device manufactured by Ontex BV. This product is indexed under FDA Product Code / Category Classification T04010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12.08.1
- Product Code / EMDN
- T04010102
- Device Name
- Heavy Incontinence Devices
- Database Sync Date
- 2026-08-09 16:29:00
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 Sensilind Complete Care From maxi 8?
The registered manufacturer of record for Sensilind Complete Care From maxi 8 is Ontex BV.
What is the Primary UDI-DI identifier for Sensilind Complete Care From maxi 8?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05414874020869.
What classification code is assigned to this device?
This device is registered under product classification code T04010102.
Similar Classification Devices (T04010102)
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