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

928 — Class I MDR by DR. H. STAMM GmbH…

MD Atlas
DR. H. STAMM GmbH Chemische Fabrik

EUDAMED last updated this device on May 16, 2022

928

++G014STZ0866

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DR. H. STAMM GmbH Chemische Fabrik
UDI-DI code: *+G0149280 *
Reference / catalog number: 928

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: DR. H. STAMM GmbH Chemische Fabrik
SRN: DE-MF-000005887
Manufacturer status: Active

Related devices

978++G014ST2403RGOn the market 916++G014ST2403RGOn the market 6037++G014ST2403RGOn the market 977++G014ST2403RGOn the market 906++G014STAG04XEOn the market

Critical warnings

5 warnings recorded — scroll inside the panel to see all entries.

CW081
EUDAMED did not publish a description for this code.
CW167
EUDAMED did not publish a description for this code.
CW416
EUDAMED did not publish a description for this code.
CW397
EUDAMED did not publish a description for this code.
CW041
EUDAMED did not publish a description for this code.

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: *+G0149280 *
Basic UDI-DI: ++G014STZ0866
Reference / catalog number: 928
Issuing entity: HIBCC

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: 5 litre
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

D0899DETERGENTS FOR MEDICAL DEVICES - OTHER

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

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.