gudid Primary ID: BR66-17508

BR Surgical, LLC (UDI BR66-17508)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The BR Surgical, LLC (Model/Catalog Number: BR66-17508) is a medical device manufactured by BR Surgical, LLC. This product is indexed under FDA Product Code / Category Classification FHA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: BR66-17508
Product Code / EMDN: FHA
Device Name: STOCKMANN Penile Clamp, 3"
Database Sync Date: 2026-08-09 09:14:09

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of BR Surgical, LLC?

The registered manufacturer of record for BR Surgical, LLC is BR Surgical, LLC.

What is the Primary UDI-DI identifier for BR Surgical, LLC?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BR66-17508.

What classification code is assigned to this device?

This device is registered under product classification code FHA.

Similar Classification Devices (FHA)

Other Devices by BR Surgical, LLC

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint