gudid Primary ID: 201-00-46

MicroAire (UDI 201-00-46)

Manufactured by Microaire Surgical Instruments LLC

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

Scannable UDI-DI Representation

Device Regulatory Overview

The MicroAire (Model/Catalog Number: 201-00-46) is a medical device manufactured by Microaire Surgical Instruments LLC. This product is indexed under FDA Product Code / Category Classification FQH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 201-00-46
Product Code / EMDN: FQH
Device Name: FEMORAL SPRAY TIP
Database Sync Date: 2026-08-09 09:05:24

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 MicroAire?

The registered manufacturer of record for MicroAire is Microaire Surgical Instruments LLC.

What is the Primary UDI-DI identifier for MicroAire?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 201-00-46.

What classification code is assigned to this device?

This device is registered under product classification code FQH.

Similar Classification Devices (FQH)

Other Devices by Microaire Surgical Instruments LLC

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