gudid
Primary ID: 9013S0042
Dantec (UDI 9013S0042)
Manufactured by NATUS MANUFACTURING LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dantec - Primary ID 9013S0042
Device Regulatory Overview
The Dantec (Model/Catalog Number: 9013S0042) is a medical device manufactured by NATUS MANUFACTURING LIMITED. This product is indexed under FDA Product Code / Category Classification IKT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9013S0042
- Product Code / EMDN
- IKT
- Device Name
- DantecTM DCN
- Database Sync Date
- 2026-08-09 09:57:21
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 Dantec?
The registered manufacturer of record for Dantec is NATUS MANUFACTURING LIMITED.
What is the Primary UDI-DI identifier for Dantec?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9013S0042.
What classification code is assigned to this device?
This device is registered under product classification code IKT.
Similar Classification Devices (IKT)
Other Devices by NATUS MANUFACTURING LIMITED
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