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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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TF-23 Clase I Tira hidrocoloide — 2 UDI-DI variants, MDR

MD Atlas
Orkla Cederroth, SAU

Data from EUDAMED, last updated May 23, 2026

TF-23 Clase I Tira hidrocoloide

8414797TF23HIDROBB

2 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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8414797TF23HIDROBB
Device name: TF-23 Clase I Tira hidrocoloide
Device model: TF-23 Clase I Tira hidrocoloide
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 28, 2023

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

2 UDI-DI variants

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Applied filters

basicUdiUlid01H8Y0FPZ9BRJHPGYXNHZ1BMTY

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

51000277108402001009747
DRSOS PU Hydrocolloid 12X608411719560693