GUDIDData
gudid Primary ID: 000

INSTRUMENT HEAD FOR UNISPEC TUBES (UDI 000)

Manufactured by Heine Optotechnik GmbH & Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for INSTRUMENT HEAD FOR UNISPEC TUBES - Primary ID 000

Device Regulatory Overview

The INSTRUMENT HEAD FOR UNISPEC TUBES (Model/Catalog Number: 000) is a medical device manufactured by Heine Optotechnik GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification FER within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
000
Product Code / EMDN
FER
Device Name
Database Sync Date
2026-08-09 09:26:12

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 INSTRUMENT HEAD FOR UNISPEC TUBES?

The registered manufacturer of record for INSTRUMENT HEAD FOR UNISPEC TUBES is Heine Optotechnik GmbH & Co. KG.

What is the Primary UDI-DI identifier for INSTRUMENT HEAD FOR UNISPEC TUBES?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 000.

What classification code is assigned to this device?

This device is registered under product classification code FER.

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