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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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Impactors — 7 UDI-DI variants, MDR (Keri Medical SA)

MD Atlas
Keri Medical SA

Data from EUDAMED, last updated May 23, 2026

Impactors

764018116018BD

7 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: Keri Medical SA

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 764018116018BD
Device name: Impactors
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Keri Medical SA
SRN: CH-MF-000021960
Country: Switzerland
Email: info@kerimedical.com
Phone: +41 58 255 01 30

Authorised representative

Name: Keri Medical France
SRN: FR-AR-000009590
Country: France

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KQC3X1A6D4NCPJ3NR0JQSV7Y

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

Cup positioner and impactor07640181161102
Neck impactor07640181161263
Offset cup holder impactor positioner07640181162093
Offset cup holder impactor positioner PLUS07640181162970
Straight cup holder impactor positioner07640181162086
Straight cup holder impactor positioner PLUS07640181163342
Straight cup positioner and impactor07640181161119