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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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Adaptacap Bottle Adapter — 6 UDI-DI variants, MDR

MD Atlas
Baxter Healthcare SA

Data from EUDAMED, last updated May 23, 2026

Adaptacap Bottle Adapter

00854120000000000000002HN

6 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

Administers medicine

Identity & classification

Basic UDI-DI: 00854120000000000000002HN
Device name: Adaptacap Bottle Adapter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 2, 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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KJQTBGBAC0WS9V4SAC8D5Y8P

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

Adaptacap25413765477335
Adaptacap25413765589359
Adaptacap20085412477859
Adaptacap20085412477811
Adaptacap20085412477767
Adaptacap20085412477835