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

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MD Atlas
Z-Systems AG

Data from EUDAMED, last updated Jun 11, 2026

DP230

B-07640166767824

1 reference

Class I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Risk category: Class I
Manufacturer: Z-Systems AG

Device family identification

Device name: DP230
Basic UDI-DI: B-07640166767824
Issuing agency: EUDAMED
Version date: Apr 29, 2026

Classification

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Risk category: Class I
Status: On the market

Manufacturer & authorised representative

Manufacturer

Name: Z-Systems AG
SRN: CH-MF-000029012
Country: Switzerland
Email: quality@zsystems.com

Authorised representative

Name: Axxos GmbH
SRN: DE-AR-000005590
Country: Germany
Phone: +41795637850

Device characteristics

Reusable

EMDN code(s)

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

Q010280Prosthetic dentistry devices - accessories

References by status

References

1 reference

Export results

Applied filters

basicUdiUlid01KQC6YMEDZ9RD75X9J384YAH6

Format

Summary

31 columns included

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
DP230	`DP230`	`07640166767824`	1	On the market