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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

30.9.0010 — IVDR Class A IVDR by GONOTEC Gesellschaft…

MD Atlas
GONOTEC Gesellschaft für Meß- und Regeltechnik mbH

EUDAMED last updated this device on Jun 20, 2024

30.9.0010

426034178SPECRECEPF8

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: GONOTEC Gesellschaft für Meß- und Regeltechnik mbH
UDI-DI code: 04260341780542
Reference / catalog number: 30.9.0010

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Manufacturer information

Organization name: GONOTEC Gesellschaft für Meß- und Regeltechnik mbH
SRN: DE-MF-000006548
Manufacturer status: Active

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# 32.02000B-04260341780672On the market # 32.00000B-04260341780658On the market # 32.12000B-04260341780689On the market # 32.BB-04260341780696On the market # 35.00B-04260341780702On the market

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: 04260341780542
Basic UDI-DI: 426034178SPECRECEPF8
Reference / catalog number: 30.9.0010
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: 1000
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W02069085VARIOUS SAMPLE PROCESSING INSTRUMENTS - CONSUMABLES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.