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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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Gauze Products — 8 UDI-DI variants, MDR (Sopharma AD)

MD Atlas
Sopharma AD

Data from EUDAMED, last updated May 23, 2026

Gauze Products

380001063200118T

8 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: 380001063200118T
Device name: Gauze Products
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 23, 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

8 UDI-DI variants

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Applied filters

basicUdiUlid01G3R5D4FV2P9QYZ9QE0NQ6E2G

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

Hygroscopic Gauze Non Sterile03800728407931
Hygroscopic Gauze Non Sterile03800728407924
Hygroscopic Gauze Non Sterile03800728407818
Hygroscopic Gauze Non Sterile03800010647014
Hygroscopic Gauze Non Sterile03800728710185
Hygroscopic Gauze Non Sterile03800010647021
Hygroscopic Gauze Non Sterile03800010647007
Hygroscopic Gauze Sterile03800728710437