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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Hammer — 12 UDI-DI variants, MDR

MD Atlas
Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.

Data from EUDAMED, last updated May 24, 2026

Hammer

5996527653HAMMERNSTDU

12 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5996527653HAMMERNSTDU
Device name: Hammer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 3, 2024

Manufacturer & authorised representative

Manufacturer

Name: Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.
SRN: HU-MF-000006772
Country: Hungary
Email: metal@sanatmetal.hu
Phone: +3636512901

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01HK7GP4A2KW1YZ1TX133KYS1B

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

ConeTact sliding hammer05996527903908
Fork Hammer05996527139185
Fork Hammer05996527026041
Fork Hammer05996527002960
Fork Hammer05996527002816
Hammer05996527002458
Hammer05996527002489
Hammer05996527002472
Hammer05996527002465
Impactor for intramedullary nail05996527021473
Slap hammer05996527022326
Sliding hammer05996527025808