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

7501883-01 — Class I MDR by Hupfer Metallwerke GmbH…

MD Atlas
Hupfer Metallwerke GmbH & Co KG

EUDAMED last updated this device on Oct 24, 2025

7501883-01

4044593SiebkoerbeNU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Hupfer Metallwerke GmbH & Co KG
UDI-DI code: 04044593017362
Reference / catalog number: 7501883-01

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: Hupfer Metallwerke GmbH & Co KG
SRN: DE-MF-000007652
Manufacturer status: Active

Related devices

75009894044593SiebkoerbeNUOn the market 75017394044593SiebkoerbeNUOn the market 75009124044593SiebkoerbeNUOn the market 75156454044593SiebkoerbeNUOn the market 75156634044593SiebkoerbeNUOn 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.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04044593017362
Basic UDI-DI: 4044593SiebkoerbeNU
Reference / catalog number: 7501883-01
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on 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)

S010401TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification