GUDIDData
gudid Primary ID: MLGS4X7AC

BEAR (UDI MLGS4X7AC)

Manufactured by Mytamed, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BEAR - Primary ID MLGS4X7AC

Device Regulatory Overview

The BEAR (Model/Catalog Number: MLGS4X7AC) is a medical device manufactured by Mytamed, Inc.. This product is indexed under FDA Product Code / Category Classification EQH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MLGS4X7AC
Product Code / EMDN
EQH
Device Name
Fiberoptic Light Cable, 7.5', Storz to ACMI
Database Sync Date
2026-08-09 09:04:03

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 BEAR?

The registered manufacturer of record for BEAR is Mytamed, Inc..

What is the Primary UDI-DI identifier for BEAR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MLGS4X7AC.

What classification code is assigned to this device?

This device is registered under product classification code EQH.

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