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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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Postoperative compressive bodysuits — 324 UDI-DI variants, MDR

MD Atlas
Tex Acces MCV S.R.L.

Data from EUDAMED, last updated May 31, 2026

Postoperative compressive bodysuits

59447591COS6D

324 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: Tex Acces MCV S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59447591COS6D
Device name: Postoperative compressive bodysuits
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: Tex Acces MCV S.R.L.
SRN: RO-MF-000029775
Country: Romania
Email: mariusvisinescu@bustieremedicale.ro
Phone: +40748219724

Variants by status

UDI-DI variants

324 UDI-DI variants

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Applied filters

basicUdiUlid01KRBFFKZAZY91784VW6J87QRP

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

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MAAM05944759121522
MAAM05944759119161
MAAM05944759119895