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.

TF-02 Clase I Tiras PE ACRIS 453 — 9 UDI-DI variants, MDR

MD Atlas
Orkla Cederroth, SAU

Data from EUDAMED, last updated May 23, 2026

TF-02 Clase I Tiras PE ACRIS 453

8414797TF02PE00S5W

9 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: Orkla Cederroth, SAU

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: 8414797TF02PE00S5W
Device name: TF-02 Clase I Tiras PE ACRIS 453
Device model: TF-02 Clase I Tiras PE ACRIS 453
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 21, 2021

Manufacturer & authorised representative

Manufacturer

Name: Orkla Cederroth, SAU
SRN: ES-MF-000003606
Country: Spain
Email: eudamed@orkla.es
Phone: +34938657810

Variants by status

UDI-DI variants

9 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

basicUdiUlid01FQEVH2D0D9Y9XDRR9VD0QT4J

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

31068508480024793102
31068708480024793171
5103002908480024793218
5103019408480000796752
DR.SOS PE Transparent Surtido EXP 12x2007310610029449
DRSOS PE Trans Surtido 12X2008411719509203
30950308411719659205
31065208424818281482
Froiz PE Beige Surtido 8X3008424818281451