eudamed_udi
Primary ID: 05600320080635
Trouxa de Extremidades (UDI 05600320080635)
Manufactured by Oasipor - Medical, S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Trouxa de Extremidades - Primary ID 05600320080635
Device Regulatory Overview
The Trouxa de Extremidades (Model/Catalog Number: 215120) is a medical device manufactured by Oasipor - Medical, S.A.. This product is indexed under FDA Product Code / Category Classification T0202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 215120
- Product Code / EMDN
- T0202
- Device Name
- Trouxas Cirúrgicas
- Database Sync Date
- 2026-08-09 16:29:13
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 Trouxa de Extremidades?
The registered manufacturer of record for Trouxa de Extremidades is Oasipor - Medical, S.A..
What is the Primary UDI-DI identifier for Trouxa de Extremidades?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05600320080635.
What classification code is assigned to this device?
This device is registered under product classification code T0202.
Similar Classification Devices (T0202)
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