eudamed_udi
Primary ID: 05600371601735
BeMate (UDI 05600371601735)
Manufactured by MULTIORTHOS LDA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BeMate - Primary ID 05600371601735
Device Regulatory Overview
The BeMate (Model/Catalog Number: BMSB33/30) is a medical device manufactured by MULTIORTHOS LDA. This product is indexed under FDA Product Code / Category Classification Y180939 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BMSB33/30
- Product Code / EMDN
- Y180939
- Device Name
- Encosto de posicionamento BeMate
- Database Sync Date
- 2026-08-09 16:29:21
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 BeMate?
The registered manufacturer of record for BeMate is MULTIORTHOS LDA.
What is the Primary UDI-DI identifier for BeMate?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05600371601735.
What classification code is assigned to this device?
This device is registered under product classification code Y180939.
Similar Classification Devices (Y180939)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint