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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

30.9.2000 — IVDD — General IVDD by GONOTEC Gesellschaft…

MD Atlas
GONOTEC Gesellschaft für Meß- und Regeltechnik mbH

EUDAMED last updated this device on Jun 7, 2023

30.9.2000

B-04260341780597

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: GONOTEC Gesellschaft für Meß- und Regeltechnik mbH
UDI-DI code: 04260341780597
Reference / catalog number: 30.9.2000

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Manufacturer information

Organization name: GONOTEC Gesellschaft für Meß- und Regeltechnik mbH
SRN: DE-MF-000006548
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: 04260341780597
Basic UDI-DI: B-04260341780597
Reference / catalog number: 30.9.2000
Issuing entity: GS1

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Calibration Standard 2000mOsmol/kg NaCl/H2O 10x 1ml for In vitro diagnostic use with all osmometers
Additional information URL: https://www.sds-id.com/1000107-3
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0101050303AQUEOUS STANDARDS (CC)

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

Related devices

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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.