GUDIDData
gudid Primary ID: Lieberman microfinger & spatula

Ambler Surgical (UDI Lieberman microfinger & spatula)

Manufactured by AMBLER SURGICAL CORP.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ambler Surgical - Primary ID Lieberman microfinger & spatula

Device Regulatory Overview

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

Technical Specifications

Model Number
Lieberman microfinger & spatula
Product Code / EMDN
HND
Device Name
Lieberman microfinger & spatula, 5 5/8'', double-ended, angled, 10.0mm from bend to tips, microfinger chopper, blunt tip, 0.5mm wide flat spatula, for use in the left hand, round handle
Database Sync Date
2026-08-09 09:01:43

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 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 Lieberman microfinger & spatula.

What classification code is assigned to this device?

This device is registered under product classification code HND.

Programmatic Export

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

JSON API Endpoint