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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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Organization name
UDI-DI code
Reference / catalog number

72004.00 / 72304.00 — Class IIa MDR by MEDIST, s.r.o.

MD Atlas
MEDIST, s.r.o.

EUDAMED last updated this device on May 5, 2026

72004.00 / 72304.00

8588009103Mevacs9W

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDIST, s.r.o.
UDI-DI code: 08588009103073
Reference / catalog number: 72004.00 / 72304.00

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View device family (Basic UDI)

Manufacturer information

Organization name: MEDIST, s.r.o.
SRN: SK-MF-000004422
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Slovakia; available across 3 countries total.

Country	On market since	Until
SlovakiaPrimary placement		Still on market
Czechia		Still on market
Poland		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08588009103073
Basic UDI-DI: 8588009103Mevacs9W
Reference / catalog number: 72004.00 / 72304.00
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Odsávačka sekrétov pre zdravotnícke zariadenia
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08588009103073

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z120105SURGICAL MEDICAL ASPIRATORS

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

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Related devices

72000.00 / 72300.008588009103Mevacs9WOn the market 72000.02 / 72300.028588009103Mevacs9WOn the market 72000.01 / 72300.018588009103Mevacs9WOn the market 72002.00 / 72002.02 / 72302.00 / 72302.028588009103Mevacs9WOn the market 72006.01 / 72006.04 / 72306.018588009103Mevacs9WOn the market

Certificates

Certificate health across this manufacturer's portfolio.

2022-MDR/QS-022Issued
Quality management systemNotified body: 2265Expiry: Sep 27, 2027