GUDIDData
eudamed_udi Primary ID: 08699258690518

NITROCARE MANUEL HASTA KARYOLASI (UDI 08699258690518)

Manufactured by NITROCARE MEDİKAL MOBİLYA SANAYİ VE TİCARET ANONİM ŞİRKETİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NITROCARE MANUEL HASTA KARYOLASI - Primary ID 08699258690518

Device Regulatory Overview

The NITROCARE MANUEL HASTA KARYOLASI (Model/Catalog Number: NITRO HB 1210) is a medical device manufactured by NITROCARE MEDİKAL MOBİLYA SANAYİ VE TİCARET ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification V080602 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
NITRO HB 1210
Product Code / EMDN
V080602
Device Name
Motorized Patient Bed
Database Sync Date
2026-08-09 16:29:20

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 NITROCARE MANUEL HASTA KARYOLASI?

The registered manufacturer of record for NITROCARE MANUEL HASTA KARYOLASI is NITROCARE MEDİKAL MOBİLYA SANAYİ VE TİCARET ANONİM ŞİRKETİ.

What is the Primary UDI-DI identifier for NITROCARE MANUEL HASTA KARYOLASI?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08699258690518.

What classification code is assigned to this device?

This device is registered under product classification code V080602.

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