gudid Primary ID: FFT02

Avalon Biomed NeoSEALER 2 Flex Flo Tips (UDI FFT02)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Avalon Biomed NeoSEALER 2 Flex Flo Tips (Model/Catalog Number: FFT02) 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: FFT02
Product Code / EMDN: EIC
Device Name: Avalon Biomed Flex Flo Tip 2 pack
Database Sync Date: 2026-08-09 09:09:51

Full Regulatory Attributes

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{
    "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 Avalon Biomed NeoSEALER 2 Flex Flo Tips?

The registered manufacturer of record for Avalon Biomed NeoSEALER 2 Flex Flo Tips is NUSMILE, LTD..

What is the Primary UDI-DI identifier for Avalon Biomed NeoSEALER 2 Flex Flo Tips?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FFT02.

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.

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