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.

Q-Flow 1 & 2 surgical light systems — 12 UDI-DI variants, MDR

MD Atlas
Merivaara Corporation

Data from EUDAMED, last updated May 23, 2026

Q-Flow 1 & 2 surgical light systems

6438435SL0001Q2

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: Merivaara Corporation

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: 6438435SL0001Q2
Device name: Q-Flow 1 & 2 surgical light systems
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 18, 2024

Manufacturer & authorised representative

Manufacturer

Name: Merivaara Corporation
SRN: FI-MF-000001175
Country: Finland
Email: merivaara@merivaara.com
Phone: +358 3 3394611

Variants by status

UDI-DI variants

12 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

basicUdiUlid01HMDV7ZSZZC56G99WZWPHYXTV

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

5201031006438435103104
5201031106438435103111
5201031206438435103128
5201033006438435103302
5201032006438435103203
5201032106438435103210
5202031006438435203101
5202031106438435203118
5202031206438435203125
5202033006438435203309
5202032006438435203200
5202032106438435203217