eudamed_udi
Primary ID: 04056839070727
S_ITE CROS SILK NX L BLK TBLU (UDI 04056839070727)
Manufactured by Signia GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for S_ITE CROS SILK NX L BLK TBLU - Primary ID 04056839070727
Device Regulatory Overview
The S_ITE CROS SILK NX L BLK TBLU (Model/Catalog Number: 10953428) is a medical device manufactured by Signia GmbH. This product is indexed under FDA Product Code / Category Classification Y214599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10953428
- Product Code / EMDN
- Y214599
- Device Name
- INSTANT FIT
- Database Sync Date
- 2026-08-09 16:29:36
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 S_ITE CROS SILK NX L BLK TBLU?
The registered manufacturer of record for S_ITE CROS SILK NX L BLK TBLU is Signia GmbH.
What is the Primary UDI-DI identifier for S_ITE CROS SILK NX L BLK TBLU?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04056839070727.
What classification code is assigned to this device?
This device is registered under product classification code Y214599.
Similar Classification Devices (Y214599)
Other Devices by Signia GmbH
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