gudid Primary ID: BF-S-1.6380-O

Single-Use Biopsy Forceps (UDI BF-S-1.6380-O)

Manufactured by MacroLux Medical Technology Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Single-Use Biopsy Forceps (Model/Catalog Number: BF-S-1.6380-O) is a medical device manufactured by MacroLux Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification HFB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: BF-S-1.6380-O
Product Code / EMDN: HFB
Device Name: Single-Use Biopsy Forceps, BF-S-1.6380-O
Database Sync Date: 2026-08-09 09:06:35

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 Single-Use Biopsy Forceps?

The registered manufacturer of record for Single-Use Biopsy Forceps is MacroLux Medical Technology Co., Ltd..

What is the Primary UDI-DI identifier for Single-Use Biopsy Forceps?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BF-S-1.6380-O.

What classification code is assigned to this device?

This device is registered under product classification code HFB.

Similar Classification Devices (HFB)

Other Devices by MacroLux Medical Technology Co., Ltd.

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