GUDIDData
eudamed_udi Primary ID: 01220000225787

Nosefrida EL ASPIRADOR NASAL (UDI 01220000225787)

Manufactured by Fridababy, LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nosefrida EL ASPIRADOR NASAL - Primary ID 01220000225787

Device Regulatory Overview

The Nosefrida EL ASPIRADOR NASAL (Model/Catalog Number: n/a) is a medical device manufactured by Fridababy, LLC. This product is indexed under FDA Product Code / Category Classification Q030199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
n/a
Product Code / EMDN
Q030199
Device Name
NoseFrida the Snotsucker
Database Sync Date
2026-08-09 16:29:18

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 Nosefrida EL ASPIRADOR NASAL?

The registered manufacturer of record for Nosefrida EL ASPIRADOR NASAL is Fridababy, LLC.

What is the Primary UDI-DI identifier for Nosefrida EL ASPIRADOR NASAL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 01220000225787.

What classification code is assigned to this device?

This device is registered under product classification code Q030199.

Programmatic Export

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

JSON API Endpoint