ANDADOR ROLLATINO PGO NEGRO (UDI 08435669510843)
Manufactured by FABRICACIONES ORTOPEDICAS ALBACETE, S.L.
Device Regulatory Overview
The ANDADOR ROLLATINO PGO NEGRO (Model/Catalog Number: 0601.3517) is a medical device manufactured by FABRICACIONES ORTOPEDICAS ALBACETE, S.L.. This product is indexed under FDA Product Code / Category Classification Y120606 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0601.3517
- Product Code / EMDN
- Y120606
- Device Name
- AIR
- Database Sync Date
- 2026-08-09 16:28:45
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 ANDADOR ROLLATINO PGO NEGRO?
The registered manufacturer of record for ANDADOR ROLLATINO PGO NEGRO is FABRICACIONES ORTOPEDICAS ALBACETE, S.L..
What is the Primary UDI-DI identifier for ANDADOR ROLLATINO PGO NEGRO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435669510843.
What classification code is assigned to this device?
This device is registered under product classification code Y120606.
Similar Classification Devices (Y120606)
Other Devices by FABRICACIONES ORTOPEDICAS ALBACETE, S.L.
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