GUDIDData
eudamed_udi Primary ID: 03760071201689

Bluetens Classic 2 (UDI 03760071201689)

Manufactured by Bluetens limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bluetens Classic 2 - Primary ID 03760071201689

Device Regulatory Overview

The Bluetens Classic 2 (Model/Catalog Number: CL2FR) is a medical device manufactured by Bluetens limited. This product is indexed under FDA Product Code / Category Classification Z12062899 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CL2FR
Product Code / EMDN
Z12062899
Device Name
Bluetens Classic 2
Database Sync Date
2026-08-09 17:21:42

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Bluetens Classic 2?

The registered manufacturer of record for Bluetens Classic 2 is Bluetens limited.

What is the Primary UDI-DI identifier for Bluetens Classic 2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760071201689.

What classification code is assigned to this device?

This device is registered under product classification code Z12062899.

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