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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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Cotton wool — 5 UDI-DI variants, MDR (Sopharma AD)

MD Atlas
Sopharma AD

Data from EUDAMED, last updated May 23, 2026

Cotton wool

3800010632091MH

5 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: 3800010632091MH
Device name: Cotton wool
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 12, 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

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GCR7KXD2TWMX9NVKTBA5H1H8

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

Cotton wool Non Sterile03800728400789
Cotton wool Non Sterile03800728400772
Cotton wool Non Sterile03800728710178
Cotton wool Non Sterile03800728400666
Cotton wool Non Sterile03800728400765