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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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Non Woven Compresses Sterile — 3 UDI-DI variants, MDR (Sopharma AD)

MD Atlas
Sopharma AD

Data from EUDAMED, last updated May 23, 2026

Non Woven Compresses Sterile

380001063200148Z

3 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: Sopharma AD

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Registered: No

Registered: No

Identity & classification

Basic UDI-DI: 380001063200148Z
Device name: Non Woven Compresses Sterile
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2022

Manufacturer & authorised representative

Manufacturer

Name: Sopharma AD
SRN: BG-MF-000019983
Country: Bulgaria
Email: mail@sopharma.bg
Phone: +35980020222

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01G3QW8ZF22P1FNY0TWPR80NE1

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

Non Woven Compresses Sterile03800728414618
Non Woven Compresses Sterile03800728414113
Non Woven Compresses Sterile03800728414311