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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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VACS II 8.0 x 20 — 1 UDI-DI variant, MDD (OSYPKA GmbH)

MD Atlas
OSYPKA GmbH

Data from EUDAMED, last updated May 31, 2026

VACS II 8.0 x 20

B-04044508109045

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class III

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Manufacturer: OSYPKA GmbH

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: CE 634279
Type: refdata.legacy.mdd-certificate-type.ii-4
Notified body: BSI Group The Netherlands B.V. (2797)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-04044508109045
Device name: —
Device model: VACS II 8.0 x 20
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: OSYPKA GmbH
SRN: DE-MF-000005610
Country: Germany
Email: ra@osypka.de
Phone: +49 7623 7405 0

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSMDKA4NA4C2GQ48VGKQKFVN

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

VACS II 8.0 x 2004044508109045