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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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STERILE GAUZE COMPRESSES 20 cm / 20 cm — 1 UDI-DI variant, MDD

MD Atlas
PRODCONFARM SRL

Data from EUDAMED, last updated May 30, 2026

STERILE GAUZE COMPRESSES 20 cm / 20 cm

B-ROMF000017975PRODCS8NA

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: PRODCONFARM SRL

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 1783- MDD-030
Type: refdata.legacy.mdd-certificate-type.v
Notified body: TURKISH STANDARDS INSTITUTION (TSE) (1783)
Validity: May 25, 2024

Identity & classification

Basic UDI-DI: B-ROMF000017975PRODCS8NA
Device name: STERILE GAUZE COMPRESSES 20 cm / 20 cm
Device model: STERILE GAUZE COMPRESSES 20 cm / 20 cm
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Jan 31, 2022

Manufacturer & authorised representative

Manufacturer

Name: PRODCONFARM SRL
SRN: RO-MF-000017975
Country: Romania
Email: prodconfarm@yahoo.com
Phone: +40248206136

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01FTQY3A2WGP927CQYHTGV7FQC

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

PROD CS 8D-ROMF000017975PRODCS8NA