GUDIDData
gudid Primary ID: Schink metatarsal spreader forceps

Ambler Surgical (UDI Schink metatarsal spreader forceps)

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 Schink metatarsal spreader forceps

Device Regulatory Overview

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

Technical Specifications

Model Number
Schink metatarsal spreader forceps
Product Code / EMDN
DWS
Device Name
Schink metatarsal spreader forceps, 5'', child size, curved, smooth jaws, ring handle, with ratchet
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
}
                            

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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 Schink metatarsal spreader forceps.

What classification code is assigned to this device?

This device is registered under product classification code DWS.

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