eudamed_udi Primary ID: M294CM1793300

Booty Bar, post-op BBL (UDI M294CM1793300)

Manufactured by CLINIMED

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Booty Bar, post-op BBL (Model/Catalog Number: CM179330) is a medical device manufactured by CLINIMED. This product is indexed under FDA Product Code / Category Classification L250399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CM179330
Product Code / EMDN: L250399
Device Name: Booty Bar, post-op BBL
Database Sync Date: 2026-08-09 16:30:12

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 Booty Bar, post-op BBL?

The registered manufacturer of record for Booty Bar, post-op BBL is CLINIMED.

What is the Primary UDI-DI identifier for Booty Bar, post-op BBL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M294CM1793300.

What classification code is assigned to this device?

This device is registered under product classification code L250399.

Similar Classification Devices (L250399)

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