gudid Primary ID: 999-DB6

BOJRAB DISSECTOR, MEDIUM, ANGLED 115 (UDI 999-DB6)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The BOJRAB DISSECTOR, MEDIUM, ANGLED 115 (Model/Catalog Number: 999-DB6) is a medical device manufactured by Grace Medical, Inc.. This product is indexed under FDA Product Code / Category Classification LRC within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2308-2026 View Full Alert →

TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis...

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Technical Specifications

Model Number: 999-DB6
Product Code / EMDN: LRC
Device Name: BOJRAB DISSECTOR, MEDIUM, ANGLED 115 0.76MM X 2.11MM STAINLESS STEEL
Database Sync Date: 2026-08-09 09:59:39

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 BOJRAB DISSECTOR, MEDIUM, ANGLED 115?

The registered manufacturer of record for BOJRAB DISSECTOR, MEDIUM, ANGLED 115 is Grace Medical, Inc..

What is the Primary UDI-DI identifier for BOJRAB DISSECTOR, MEDIUM, ANGLED 115?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 999-DB6.

What classification code is assigned to this device?

This device is registered under product classification code LRC.

Similar Classification Devices (LRC)

Other Devices by Grace Medical, Inc.

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