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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

888999 — IVDR Class A IVDR by Hamilton Bonaduz AG

MD Atlas
Hamilton Bonaduz AG

EUDAMED last updated this device on Sep 26, 2024

888999

076300326888999DE

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Hamilton Bonaduz AG
UDI-DI code: 07630032663848
Reference / catalog number: 888999

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Manufacturer information

Organization name: Hamilton Bonaduz AG
SRN: CH-MF-000013585
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 07630032663848
Basic UDI-DI: 076300326888999DE
Reference / catalog number: 888999
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: 1x 235948 CO-RE Tips Filter (50µL) 2x 235903 CO-RE Tips Filter (300µL) 1x 235905 CO-RE Tips Filter (1000µL)
Additional information URL: https://www.hamiltoncompany.com/de
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0580IVD GENERAL USE CONSUMABLES DEVICES - OTHER ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
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Serial number
Software identification

Certificates

Certificate health across this manufacturer's portfolio.

HX 1774385-1Issued
refdata.certificate-ivdr-type.quality-management-systemNotified body: 0197Expiry: Sep 15, 2029

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