gudid Primary ID: P-219-MRI

AincA (UDI P-219-MRI)

Manufactured by ANESTHESIA ASSOCIATES, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AincA (Model/Catalog Number: P-219-MRI) is a medical device manufactured by ANESTHESIA ASSOCIATES, INC.. This product is indexed under FDA Product Code / Category Classification CAP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: P-219-MRI
Product Code / EMDN: CAP
Device Name: Gauge, Pressure, Replacement, MRI Cond 3T, 0-60 psi, 1/8" NPT-M Bottom, 1.5" Dia, for 00-325-MRI JetVent
Database Sync Date: 2026-08-09 09:16:44

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 AincA?

The registered manufacturer of record for AincA is ANESTHESIA ASSOCIATES, INC..

What is the Primary UDI-DI identifier for AincA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P-219-MRI.

What classification code is assigned to this device?

This device is registered under product classification code CAP.

Similar Classification Devices (CAP)

Other Devices by ANESTHESIA ASSOCIATES, INC.

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