GUDIDData
gudid Primary ID: 18-13301-0001

SnuggleFit (UDI 18-13301-0001)

Manufactured by DYMEDIX DIAGNOSTICS, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SnuggleFit - Primary ID 18-13301-0001

Device Regulatory Overview

The SnuggleFit (Model/Catalog Number: 18-13301-0001) is a medical device manufactured by DYMEDIX DIAGNOSTICS, INC.. This product is indexed under FDA Product Code / Category Classification BZQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
18-13301-0001
Product Code / EMDN
BZQ
Device Name
SnuggleFit Infant Effort Belt - Alice 5
Database Sync Date
2026-08-09 09:31:20

Full Regulatory Attributes

🔒 Token Gated
{
    "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 SnuggleFit?

The registered manufacturer of record for SnuggleFit is DYMEDIX DIAGNOSTICS, INC..

What is the Primary UDI-DI identifier for SnuggleFit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 18-13301-0001.

What classification code is assigned to this device?

This device is registered under product classification code BZQ.

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