eudamed_udi
Primary ID: 06973596010521
Bendiboard (UDI 06973596010521)
Manufactured by Conlett Technology Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bendiboard - Primary ID 06973596010521
Device Regulatory Overview
The Bendiboard (Model/Catalog Number: BB001) is a medical device manufactured by Conlett Technology Inc. This product is indexed under FDA Product Code / Category Classification Y060699 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BB001
- Product Code / EMDN
- Y060699
- Device Name
- Bendiboard
- Database Sync Date
- 2026-08-09 16:51:56
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 Bendiboard?
The registered manufacturer of record for Bendiboard is Conlett Technology Inc.
What is the Primary UDI-DI identifier for Bendiboard?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973596010521.
What classification code is assigned to this device?
This device is registered under product classification code Y060699.
Similar Classification Devices (Y060699)
Other Devices by Conlett Technology Inc
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint