gudid Primary ID: W Version

Grin App -W (UDI W Version)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Grin App -W (Model/Catalog Number: W Version) is a medical device manufactured by Get-Grin Inc.. This product is indexed under FDA Product Code / Category Classification LMD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: W Version
Product Code / EMDN: LMD
Device Name
Database Sync Date: 2026-08-09 09:01:11

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 Grin App -W?

The registered manufacturer of record for Grin App -W is Get-Grin Inc..

What is the Primary UDI-DI identifier for Grin App -W?

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

What classification code is assigned to this device?

This device is registered under product classification code LMD.

Similar Classification Devices (LMD)

Other Devices by Get-Grin Inc.

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