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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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Tampon Compressifs — 7 UDI-DI variants, MDR (SECURIMED)

MD Atlas
SECURIMED

Data from EUDAMED, last updated May 19, 2026

Tampon Compressifs

37011402compressifsPH

7 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: SECURIMED

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37011402compressifsPH
Device name: Tampon Compressifs
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 23, 2023

Manufacturer & authorised representative

Manufacturer

Name: SECURIMED
SRN: FR-MF-000006782
Country: France
Email: info@securimed.fr
Phone: 03.28.64.75.45

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01H14EVHD9ZWXSQSQPY230VTY5

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

HAEMOBAND03701140200219
HAEMOBAND03701140200936
497103701140200905
486003701140200158
496503701140200929
497003701140200165
496603701140200912