eudamed_udi
Primary ID: +D7701180913
KIT D.B.E. SYSTEM (UDI +D7701180913)
Manufactured by SWEDEN & MARTINA S.P.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KIT D.B.E. SYSTEM - Primary ID +D7701180913
Device Regulatory Overview
The KIT D.B.E. SYSTEM (Model/Catalog Number: ESP-G-KIT-INT) is a medical device manufactured by SWEDEN & MARTINA S.P.A.. This product is indexed under FDA Product Code / Category Classification L159099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ESP-G-KIT-INT
- Product Code / EMDN
- L159099
- Device Name
- 0006
- Database Sync Date
- 2026-08-09 16:29:10
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 KIT D.B.E. SYSTEM?
The registered manufacturer of record for KIT D.B.E. SYSTEM is SWEDEN & MARTINA S.P.A..
What is the Primary UDI-DI identifier for KIT D.B.E. SYSTEM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +D7701180913.
What classification code is assigned to this device?
This device is registered under product classification code L159099.
Similar Classification Devices (L159099)
Other Devices by SWEDEN & MARTINA S.P.A.
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