GUDIDData
gudid Primary ID: DSAEK descemet's membrane stripper replacement handle only

Ambler Surgical (UDI DSAEK descemet's membrane stripper replacement handle only)

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 DSAEK descemet's membrane stripper replacement handle only

Device Regulatory Overview

The Ambler Surgical (Model/Catalog Number: DSAEK descemet's membrane stripper replacement handle only) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification KYG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DSAEK descemet's membrane stripper replacement handle only
Product Code / EMDN
KYG
Device Name
DSAEK descemet's membrane stripper replacement handle only, 3 7/8'', round handle, for use with 2121E and 2122E tips
Database Sync Date
2026-08-09 09:01:49

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 DSAEK descemet's membrane stripper replacement handle only.

What classification code is assigned to this device?

This device is registered under product classification code KYG.

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