GUDIDData
gudid Primary ID: 71229

FreeStyle InsuLinx (UDI 71229)

Manufactured by ABBOTT DIABETES CARE INC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FreeStyle InsuLinx - Primary ID 71229

Device Regulatory Overview

The FreeStyle InsuLinx (Model/Catalog Number: 71229) is a medical device manufactured by ABBOTT DIABETES CARE INC. This product is indexed under FDA Product Code / Category Classification LFR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
71229
Product Code / EMDN
LFR
Device Name
FreeStyle InsuLinx Blood Glucose Test Strips
Database Sync Date
2026-08-09 09:04:18

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 FreeStyle InsuLinx?

The registered manufacturer of record for FreeStyle InsuLinx is ABBOTT DIABETES CARE INC.

What is the Primary UDI-DI identifier for FreeStyle InsuLinx?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 71229.

What classification code is assigned to this device?

This device is registered under product classification code LFR.

Programmatic Export

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

JSON API Endpoint