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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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Maquet Sterigrip — 3 UDI-DI variants, MDR (Maquet SAS)

MD Atlas
Maquet SAS

Data from EUDAMED, last updated May 19, 2026

Maquet Sterigrip

3700712421229R8

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: Maquet SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3700712421229R8
Device name: Maquet Sterigrip
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 8, 2022

Manufacturer & authorised representative

Manufacturer

Name: Maquet SAS
SRN: FR-MF-000002926
Country: France
Email: sylviane.boironbourgeois@getinge.com
Phone: +33 6 08 73 60 40

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01G9YDFHY0KBQMH5FPJ316YXYC

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

ARD56791790003700712405137
ARD56720390003700712405120
ARD56720390103700712405144