eudamed_udi
Primary ID: 05600456960115
Eclipse (UDI 05600456960115)
Manufactured by Orthos XXI, Unipessoal Lda
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Eclipse - Primary ID 05600456960115
Device Regulatory Overview
The Eclipse (Model/Catalog Number: 56GR3ELCP150) is a medical device manufactured by Orthos XXI, Unipessoal Lda. This product is indexed under FDA Product Code / Category Classification V0805030102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 56GR3ELCP150
- Product Code / EMDN
- V0805030102
- Device Name
- Grua de Transferência
- 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 Eclipse?
The registered manufacturer of record for Eclipse is Orthos XXI, Unipessoal Lda.
What is the Primary UDI-DI identifier for Eclipse?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05600456960115.
What classification code is assigned to this device?
This device is registered under product classification code V0805030102.
Similar Classification Devices (V0805030102)
Other Devices by Orthos XXI, Unipessoal Lda
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