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

121-001 — IVDR Class A IVDR by Sanowa PlastoTec GmbH

MD Atlas
Sanowa PlastoTec GmbH

EUDAMED last updated this device on Nov 13, 2025

121-001

4099853004A9

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Sanowa PlastoTec GmbH
UDI-DI code: 04099853003951
Reference / catalog number: 121-001

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: Sanowa PlastoTec GmbH
SRN: DE-MF-000040380
Manufacturer status: Active

Related devices

165-0164099853001A3On the market 165-0164099853001A3On the market Bio Net 2 Embedding cassette - beige (loose)4099853001A3On the market Bio Net 2 Embedding cassette - beige (loose)4099853001A3On the market Bio Net 2 Embedding cassette - blue (loose)4099853001A3On 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: 04099853003951
Basic UDI-DI: 4099853004A9
Reference / catalog number: 121-001
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: 4000
Additional product description: —
Additional information URL: https://www.sanowa-plastotec.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W05030501INCLUSION DEVICES, CASSETTES

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.