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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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GRI-FILL PERISTALTIC SET — 2 UDI-DI variants, MDR

MD Atlas
Laboratorios Grifols S.A.

Data from EUDAMED, last updated May 23, 2026

GRI-FILL PERISTALTIC SET

8437017294A070003NB

2 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: Laboratorios Grifols S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8437017294A070003NB
Device name: GRI-FILL PERISTALTIC SET
Device model: Eur.Sur
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 15, 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

2 UDI-DI variants

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Applied filters

basicUdiUlid01GP1D06X0EW4M9CJ7TTAQXEMX

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

73501708437017294009
73501908437017294016