gudid Primary ID: ZFFT40

Flex Flo Tips 40 units (UDI ZFFT40)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Flex Flo Tips 40 units (Model/Catalog Number: ZFFT40) is a medical device manufactured by NUSMILE, LTD.. This product is indexed under FDA Product Code / Category Classification EIC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ZFFT40
Product Code / EMDN: EIC
Device Name: Flex Flo Tips 40 units
Database Sync Date: 2026-08-09 09:12:28

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 Flex Flo Tips 40 units?

The registered manufacturer of record for Flex Flo Tips 40 units is NUSMILE, LTD..

What is the Primary UDI-DI identifier for Flex Flo Tips 40 units?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ZFFT40.

What classification code is assigned to this device?

This device is registered under product classification code EIC.

Similar Classification Devices (EIC)

Other Devices by NUSMILE, LTD.

Programmatic Export

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

JSON API Endpoint