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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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Adhesive non-woven fabric — 6 UDI-DI variants, MDR

MD Atlas
Iberhospitex, S.A.

Data from EUDAMED, last updated May 23, 2026

Adhesive non-woven fabric

8428097TAPE99

6 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: Iberhospitex, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8428097TAPE99
Device name: Adhesive non-woven fabric
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 16, 2021

Manufacturer & authorised representative

Manufacturer

Name: Iberhospitex, S.A.
SRN: ES-MF-000000160
Country: Spain
Email: info@iht.es
Phone: +34938436034

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01FMH9S5E6XXPHCYTQE5NWF29W

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

003221008428097878807
003223008428097878609
003224008428097879101
003225008428097878906
003226008428097879002
003222008428097878500