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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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Template — 6 UDI-DI variants, MDR (Keri Medical SA)

MD Atlas
Keri Medical SA

Data from EUDAMED, last updated May 23, 2026

Template

764018116004B2

6 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764018116004B2
Device name: Template
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 25, 2024

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

6 UDI-DI variants

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Applied filters

basicUdiUlid01J171R8TQ8XVD69665BZP4SZN

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

KeriFlex template MCP07640181162031
KeriFlex template PIP07640181162048
KeriFuse template07640181162055
TOUCH cup template07640181162079
TOUCH PLUS cup template07640181163380
TOUCH Stem Template07640181162062