Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Rack/lid KeriFlex — 8 UDI-DI variants, MDR (Keri Medical SA)

MD Atlas
Keri Medical SA

Data from EUDAMED, last updated May 23, 2026

Rack/lid KeriFlex

764018116008BA

8 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764018116008BA
Device name: Rack/lid KeriFlex
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

8 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01J17MZRVXEBJ2CRA5SNGQEBXA

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

Lid MCP07640181162239
Lid MCP07640181161843
Lid PIP07640181162215
Lid PIP07640181161836
Rack MCP07640181161591
Rack MCP07640181162222
Rack PIP07640181162208
Rack PIP07640181161584