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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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Bottle Adapter — 5 UDI-DI variants, MDR (Baxter Healthcare SA)

MD Atlas
Baxter Healthcare SA

Data from EUDAMED, last updated May 23, 2026

Bottle Adapter

00854120000000000000078JP

5 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: Baxter Healthcare SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 00854120000000000000078JP
Device name: Bottle Adapter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 13, 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 Belgium SRL
SRN: BE-AR-000006568
Country: Belgium
Phone: +32 68 27 2211

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KHCBTESE69BYCSJNJY0JP4K2

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

Press-In-Bottle-Adapter20682126242027
Press-In-Bottle-Adapter20085412482464
Press-In-Bottle-Adapter25413765589328
Press-In-Bottle-Adapter20085412477668
Press-In-Bottle-Adapter25413765589311