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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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Organization name
UDI-DI code
Reference / catalog number

Adaptacap — Class I MDR by Baxter Healthcare SA

MD Atlas
Baxter Healthcare SA

EUDAMED last updated this device on Mar 2, 2026

Adaptacap

00854120000000000000002HN

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Baxter Healthcare SA
UDI-DI code: 25413765477335
Reference / catalog number: H9385102

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Manufacturer information

Organization name: Baxter Healthcare SA
SRN: CH-MF-000026124
Manufacturer status: Active

Related devices

Adaptacap00854120000000000000002HNOn the market Adaptacap00854120000000000000002HNOn the market Adaptacap00854120000000000000002HNOn the market Adaptacap00854120000000000000002HNOn the market Adaptacap00854120000000000000002HNOn the market

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW007
EUDAMED did not publish a description for this code.
CW011
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 3 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Norway		Still on market
Sweden		Still on market

Device identification

Trade name: Adaptacap
UDI-DI code: 25413765477335
Basic UDI-DI: 00854120000000000000002HN
Reference / catalog number: H9385102
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 20
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 20 MU50

EMDN nomenclature code(s)

A0799ADAPTERS, CONNECTORS, RAMPS, STOPCOCKS, CAPS - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

Certificate health across this manufacturer's portfolio.

G10 056740 0065Issued
Quality management systemNotified body: 0123Expiry: Nov 6, 2029
G10 056740 0072Issued
Quality management systemNotified body: 0123Expiry: Nov 5, 2029
G10 056740 0047Issued
Quality management systemNotified body: 0123Expiry: Oct 24, 2029
G10 056740 0071Issued
Quality management systemNotified body: 0123Expiry: Sep 2, 2029
G10 056740 0057Issued
Quality management systemNotified body: 0123Expiry: May 7, 2029
G10 056740 0037

Issued

Quality management systemNotified body: 0123Expiry: Mar 21, 2029