eudamed_udi
Primary ID: 05600456930774
C1 Integral (UDI 05600456930774)
Manufactured by Orthos XXI, Unipessoal Lda
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for C1 Integral - Primary ID 05600456930774
Device Regulatory Overview
The C1 Integral (Model/Catalog Number: 52CN22AFPMZZ) is a medical device manufactured by Orthos XXI, Unipessoal Lda. This product is indexed under FDA Product Code / Category Classification Y12030601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 52CN22AFPMZZ
- Product Code / EMDN
- Y12030601
- Device Name
- Auxiliares de Marcha - Canadiana
- Database Sync Date
- 2026-08-09 16:29:04
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 C1 Integral?
The registered manufacturer of record for C1 Integral is Orthos XXI, Unipessoal Lda.
What is the Primary UDI-DI identifier for C1 Integral?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05600456930774.
What classification code is assigned to this device?
This device is registered under product classification code Y12030601.
Similar Classification Devices (Y12030601)
Other Devices by Orthos XXI, Unipessoal Lda
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