GUDIDData
eudamed_udi Primary ID: 08698870325747

Reusable NIBP Cuff (UDI 08698870325747)

Manufactured by METKO MEDİKAL VE TIBBİ CİHAZLAR DIŞ TİCARET SANAYİ ANONİM ŞİRKETİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Reusable NIBP Cuff - Primary ID 08698870325747

Device Regulatory Overview

The Reusable NIBP Cuff (Model/Catalog Number: FMT-SB2) is a medical device manufactured by METKO MEDİKAL VE TIBBİ CİHAZLAR DIŞ TİCARET SANAYİ ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification Z1203020302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FMT-SB2
Product Code / EMDN
Z1203020302
Device Name
Reusable NIBP Cuff
Database Sync Date
2026-08-09 16:28:56

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 Reusable NIBP Cuff?

The registered manufacturer of record for Reusable NIBP Cuff is METKO MEDİKAL VE TIBBİ CİHAZLAR DIŞ TİCARET SANAYİ ANONİM ŞİRKETİ.

What is the Primary UDI-DI identifier for Reusable NIBP Cuff?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698870325747.

What classification code is assigned to this device?

This device is registered under product classification code Z1203020302.

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