GUDIDData
eudamed_udi Primary ID: 08682549520199

NORMMED KNEE PROSTHESIS PS CEMENTED FEMORAL COMPONENT / CoCrMo - RIGHT-6 (UDI 08682549520199)

Manufactured by NORMMED MEDİKAL SAN. VE TİC. A.Ş.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NORMMED KNEE PROSTHESIS PS CEMENTED FEMORAL COMPONENT / CoCrMo - RIGHT-6 - Primary ID 08682549520199

Device Regulatory Overview

The NORMMED KNEE PROSTHESIS PS CEMENTED FEMORAL COMPONENT / CoCrMo - RIGHT-6 (Model/Catalog Number: NMDPF46) is a medical device manufactured by NORMMED MEDİKAL SAN. VE TİC. A.Ş.. This product is indexed under FDA Product Code / Category Classification P0909030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
NMDPF46
Product Code / EMDN
P0909030101
Device Name
NORMMED KNEE PROSTHESIS PS CEMENTED FEMORAL COMPONENT / CoCrMo - RIGHT-6
Database Sync Date
2026-08-09 16:28:49

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 NORMMED KNEE PROSTHESIS PS CEMENTED FEMORAL COMPONENT / CoCrMo - RIGHT-6?

The registered manufacturer of record for NORMMED KNEE PROSTHESIS PS CEMENTED FEMORAL COMPONENT / CoCrMo - RIGHT-6 is NORMMED MEDİKAL SAN. VE TİC. A.Ş..

What is the Primary UDI-DI identifier for NORMMED KNEE PROSTHESIS PS CEMENTED FEMORAL COMPONENT / CoCrMo - RIGHT-6?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682549520199.

What classification code is assigned to this device?

This device is registered under product classification code P0909030101.

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