gudid Primary ID: Micro sharp forceps

Ambler Surgical (UDI Micro sharp forceps)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Ambler Surgical (Model/Catalog Number: Micro sharp forceps) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification GEN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Micro sharp forceps
Product Code / EMDN: GEN
Device Name: Micro sharp forceps, 2 7/8'', straight shafts with 0.10mm wide TC-dusted sharp tips with 4mm platforms, flat knurled handle
Database Sync Date: 2026-08-09 09:01:44

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 Ambler Surgical?

The registered manufacturer of record for Ambler Surgical is AMBLER SURGICAL CORP..

What is the Primary UDI-DI identifier for Ambler Surgical?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Micro sharp forceps.

What classification code is assigned to this device?

This device is registered under product classification code GEN.

Similar Classification Devices (GEN)

Other Devices by AMBLER SURGICAL CORP.

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