eudamed_udi
Primary ID: 03111790068952
BIFLEX LL 16+ (UDI 03111790068952)
Manufactured by THUASNE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BIFLEX LL 16+ - Primary ID 03111790068952
Device Regulatory Overview
The BIFLEX LL 16+ (Model/Catalog Number: 16001200840002) is a medical device manufactured by THUASNE. This product is indexed under FDA Product Code / Category Classification M0304010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 16001200840002
- Product Code / EMDN
- M0304010102
- Device Name
- Biflex Hôpital 16+
- Database Sync Date
- 2026-08-09 16:44:59
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 BIFLEX LL 16+?
The registered manufacturer of record for BIFLEX LL 16+ is THUASNE.
What is the Primary UDI-DI identifier for BIFLEX LL 16+?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03111790068952.
What classification code is assigned to this device?
This device is registered under product classification code M0304010102.
Similar Classification Devices (M0304010102)
Other Devices by THUASNE
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint