eudamed_udi
Primary ID: 05391549480060
ReShell (UDI 05391549480060)
Manufactured by LC Seating LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ReShell - Primary ID 05391549480060
Device Regulatory Overview
The ReShell (Model/Catalog Number: Back Size 2) is a medical device manufactured by LC Seating LTD. This product is indexed under FDA Product Code / Category Classification Y180999 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Back Size 2
- Product Code / EMDN
- Y180999
- Device Name
- ReShell
- Database Sync Date
- 2026-08-09 16:47:14
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ReShell?
The registered manufacturer of record for ReShell is LC Seating LTD.
What is the Primary UDI-DI identifier for ReShell?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05391549480060.
What classification code is assigned to this device?
This device is registered under product classification code Y180999.
Similar Classification Devices (Y180999)
Other Devices by LC Seating LTD
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint