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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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FlexFlo Bags Sterile water for… — 6 UDI-DI variants, MDR

MD Atlas
Baxter Healthcare SA

Data from EUDAMED, last updated May 23, 2026

FlexFlo Bags Sterile water for irrigation

0085412GMN00000000002206X

6 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Baxter Healthcare SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0085412GMN00000000002206X
Device name: FlexFlo Bags Sterile water for irrigation
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jan 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: Baxter Healthcare SA
SRN: CH-MF-000026124
Country: Switzerland
Email: simone_diorio@baxter.com
Phone: +41 (79) 4413671

Authorised representative

Name: Baxter Deutschland GmbH
SRN: DE-AR-000010308
Country: Germany
Phone: +49 89 317010

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KFBBN3W7ZZ98NKM2BM2N8125

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

FlexFlo05413760169712
FlexFlo05413760231396
FlexFlo05413760169705
FlexFlo05413760231402
FlexFlo05413760231341
FlexFlo05413760231334