eudamed_udi
Primary ID: +G399CTCIB130Z
Composite (UDI +G399CTCIB130Z)
Manufactured by CROSSTEX (PRIVATE) LIMITED.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Composite - Primary ID +G399CTCIB130Z
Device Regulatory Overview
The Composite (Model/Catalog Number: CT-CIB13) is a medical device manufactured by CROSSTEX (PRIVATE) LIMITED.. This product is indexed under FDA Product Code / Category Classification Q01010199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CT-CIB13
- Product Code / EMDN
- Q01010199
- Device Name
- Composite
- Database Sync Date
- 2026-08-09 16:30:20
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 Composite?
The registered manufacturer of record for Composite is CROSSTEX (PRIVATE) LIMITED..
What is the Primary UDI-DI identifier for Composite?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G399CTCIB130Z.
What classification code is assigned to this device?
This device is registered under product classification code Q01010199.
Similar Classification Devices (Q01010199)
Other Devices by CROSSTEX (PRIVATE) LIMITED.
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