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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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Vacuflasc — 6 UDI-DI variants, MDR (Laboratorios Grifols S.A.)

MD Atlas
Laboratorios Grifols S.A.

Data from EUDAMED, last updated May 23, 2026

Vacuflasc

8437017294A060001MU

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Laboratorios Grifols S.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8437017294A060001MU
Device name: Vacuflasc
Device model: 100 ml
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: Laboratorios Grifols S.A.
SRN: ES-MF-000000767
Country: Spain
Email: laboratorios@grifols.com
Phone: +34 935 710 100

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JZJM8H4ZNPREH4QVVBM8RP9H

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

73497208437017294108
73497308437017294115
73497608437017294146
73497108437017294023
73497508437017294139
73497408437017294122