eudamed_udi
Primary ID: 08435025935877
CEINTURE LOMBOBELT RENFORT NOIR H21 T3 (UDI 08435025935877)
Manufactured by Orliman, S.L.U.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CEINTURE LOMBOBELT RENFORT NOIR H21 T3 - Primary ID 08435025935877
Device Regulatory Overview
The CEINTURE LOMBOBELT RENFORT NOIR H21 T3 (Model/Catalog Number: TR0215213) is a medical device manufactured by Orliman, S.L.U.. This product is indexed under FDA Product Code / Category Classification Y060308 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TR0215213
- Product Code / EMDN
- Y060308
- Device Name
- RACHIS LOMBAIRE
- Database Sync Date
- 2026-08-09 16:28:48
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 CEINTURE LOMBOBELT RENFORT NOIR H21 T3?
The registered manufacturer of record for CEINTURE LOMBOBELT RENFORT NOIR H21 T3 is Orliman, S.L.U..
What is the Primary UDI-DI identifier for CEINTURE LOMBOBELT RENFORT NOIR H21 T3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435025935877.
What classification code is assigned to this device?
This device is registered under product classification code Y060308.
Similar Classification Devices (Y060308)
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