GUDIDData
eudamed_udi Primary ID: 03760071201597

Pinktens (UDI 03760071201597)

Manufactured by Bluetens limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pinktens - Primary ID 03760071201597

Device Regulatory Overview

The Pinktens (Model/Catalog Number: CL2P_UNI) 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
CL2P_UNI
Product Code / EMDN
Z12062899
Device Name
Bluetens Classic 2
Database Sync Date
2026-08-09 16:29:16

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 Pinktens?

The registered manufacturer of record for Pinktens is Bluetens limited.

What is the Primary UDI-DI identifier for Pinktens?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760071201597.

What classification code is assigned to this device?

This device is registered under product classification code Z12062899.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint