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

570 3000.322 — IVDR Class A IVDR by Eppendorf SE

MD Atlas
Eppendorf SE

EUDAMED last updated this device on Jul 24, 2024

570 3000.322

04043758-IA-CEN-005-P4

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Eppendorf SE
UDI-DI code: 04043758017285
Reference / catalog number: 570 3000.322

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: Eppendorf SE
SRN: DE-MF-000006237
Manufacturer status: Active

Related devices

5401 000.01304043758-IA-CEN-011-NVOn the market 5420 000.01604043758-IA-CEN-008-PDOn the market 5420 000.21004043758-IA-CEN-008-PDOn the market 5405 000.15804043758-IA-CEN-009-PGOn the market 5405 000.41704043758-IA-CEN-009-PGOn 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: 04043758017285
Basic UDI-DI: 04043758-IA-CEN-005-P4
Reference / catalog number: 570 3000.322
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W02069003CENTRIFUGES

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.