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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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Vaginal Specimen Sampling Product — 3 UDI-DI variants, MDR

MD Atlas
Cetro Medical AB

Data from EUDAMED, last updated May 30, 2026

Vaginal Specimen Sampling Product

7340194311009D

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: Cetro Medical AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7340194311009D
Device name: Vaginal Specimen Sampling Product
Device model: 1100
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 13, 2025

Manufacturer & authorised representative

Manufacturer

Name: Cetro Medical AB
SRN: SE-MF-000012172
Country: Sweden
Email: info@cetromedical.se
Phone: +4637133030

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01JHFFEHR13A2EZF2MA3YHWZXP

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

117007340194300221
CETRO® Brush+07340194300283
CETRO® Spatula07340194302102