eudamed_udi
Primary ID: 04063006015443
KIT STYLETTO 7X US DEMO BLK BLKG (UDI 04063006015443)
Manufactured by Signia GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KIT STYLETTO 7X US DEMO BLK BLKG - Primary ID 04063006015443
Device Regulatory Overview
The KIT STYLETTO 7X US DEMO BLK BLKG (Model/Catalog Number: 11000401) is a medical device manufactured by Signia GmbH. This product is indexed under FDA Product Code / Category Classification Y2145060102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 11000401
- Product Code / EMDN
- Y2145060102
- Device Name
- SLIM RIC
- Database Sync Date
- 2026-08-09 16:29:05
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 STYLETTO 7X US DEMO BLK BLKG?
The registered manufacturer of record for KIT STYLETTO 7X US DEMO BLK BLKG is Signia GmbH.
What is the Primary UDI-DI identifier for KIT STYLETTO 7X US DEMO BLK BLKG?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04063006015443.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060102.
Similar Classification Devices (Y2145060102)
Other Devices by Signia GmbH
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