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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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TD 13 — 2 UDI-DI variants, MDR (Orkla Wound Care AB)

MD Atlas
Orkla Wound Care AB

Data from EUDAMED, last updated May 31, 2026

TD 13

73106100130032

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Orkla Wound Care AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73106100130032
Device name: TD 13
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: Orkla Wound Care AB
SRN: SE-MF-000021041
Country: Sweden
Email: firstaid@cederroth.com
Phone: +46 10 142 64 00

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JQ8XKGXYCYPZMJ5Q9CRPAAT7

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

5100001607310610010669
5103016607310610020774