GUDIDData
gudid Primary ID: 27056EA

n.a. (UDI 27056EA)

Manufactured by Karl Storz GmbH & Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for n.a. - Primary ID 27056EA

Device Regulatory Overview

The n.a. (Model/Catalog Number: 27056EA) is a medical device manufactured by Karl Storz GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification FJL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
27056EA
Product Code / EMDN
FJL
Device Name
LASER Guide Probe, 0.8 mm
Database Sync Date
2026-08-09 09:11:33

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 n.a.?

The registered manufacturer of record for n.a. is Karl Storz GmbH & Co. KG.

What is the Primary UDI-DI identifier for n.a.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 27056EA.

What classification code is assigned to this device?

This device is registered under product classification code FJL.

Similar Classification Devices (FJL)

Other Devices by Karl Storz GmbH & Co. KG

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