Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

30.9.0850 — IVDD — General IVDD by GONOTEC Gesellschaft…

MD Atlas
GONOTEC Gesellschaft für Meß- und Regeltechnik mbH

EUDAMED last updated this device on Jun 7, 2023

30.9.0850

B-04260341780580

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: 04260341780580
Reference / catalog number: 30.9.0850

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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: 04260341780580
Basic UDI-DI: B-04260341780580
Reference / catalog number: 30.9.0850
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 850mOsmol/kg NaCl/H2O 10 x 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

# 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

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.