eudamed_udi
Primary ID: 05607283202029
Intimus L Plus 40 (UDI 05607283202029)
Manufactured by Nunex Worldwide, SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Intimus L Plus 40 - Primary ID 05607283202029
Device Regulatory Overview
The Intimus L Plus 40 (Model/Catalog Number: NNX202029) is a medical device manufactured by Nunex Worldwide, SA. This product is indexed under FDA Product Code / Category Classification T04010103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NNX202029
- Product Code / EMDN
- T04010103
- Device Name
- Premium Care
- Database Sync Date
- 2026-08-09 16:45:46
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 Intimus L Plus 40?
The registered manufacturer of record for Intimus L Plus 40 is Nunex Worldwide, SA.
What is the Primary UDI-DI identifier for Intimus L Plus 40?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05607283202029.
What classification code is assigned to this device?
This device is registered under product classification code T04010103.
Similar Classification Devices (T04010103)
Other Devices by Nunex Worldwide, SA
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