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.

SARA FLEX — 273 UDI-DI variants, MDR (ArjoHuntleigh AB)

MD Atlas
ArjoHuntleigh AB

Data from EUDAMED, last updated May 30, 2026

SARA FLEX

5060693520112VK

273 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: ArjoHuntleigh AB

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

Active device

Identity & classification

Basic UDI-DI: 5060693520112VK
Device name: SARA FLEX
Device model: HEB0000
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 19, 2024

Manufacturer & authorised representative

Manufacturer

Name: ArjoHuntleigh AB
SRN: SE-MF-000000696
Country: Sweden
Email: info@arjo.com
Phone: +46 10 335 4500

Variants by status

UDI-DI variants

273 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

basicUdiUlid01J357CHEVSYS7WG2WQ96W5TWT

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

KMCSXN-3605056097363080
KMCSXN-D-DK05055982794060
KMCSXN-2505055982767989
KMCSXN-D-2105056097320724
KMCLXN-C-4605059441296744
KMCSXN-D-0905055982768412
KMCSXN-0605055982767835
KMCSXN-D-9905055982768610
KMCSXE-D-0605055982767552
KMCLXN-1705055982764582
KMCLXN-C-0305055982764728
KMCSXE-0305055982766982
KMCSXN-4605059441296713
KMCEXN-1505055982763189
KMCSXN-C-0905055982768139
KMCEXN-D-1705055982763479
KMCLXN-D-1205055982765084
KMCSXE-C-0705055982767293
KMCEXN-D-0705055982763387
KMCSXE-9905055982767224
KMCSXN-D-1005055982768429
KMCEXN-D-1605055982763462
KMCSXE-D-1005055982767590
KMCSXN-D-PL05055982794114
KMCLXN-C-1805055982764865

3 4 5 6 7