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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

99.000.22.799 — Class IIa MDR by BISMED, s.r.o.

MD Atlas
BISMED, s.r.o.

EUDAMED last updated this device on Jan 30, 2026

99.000.22.799

859419979REDONXH

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BISMED, s.r.o.
UDI-DI code: 18594199790174
Reference / catalog number: 99.000.22.799

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Manufacturer information

Organization name: BISMED, s.r.o.
SRN: CZ-MF-000040871
Manufacturer status: Active

Related devices

05.000.22.803859419979REDONXHOn the market 05.000.22.798859419979REDONXHOn the market 05.000.22.801859419979REDONXHOn the market 99.000.22.800859419979REDONXHOn the market 99.000.22.798859419979REDONXHOn the market

Critical warnings

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

CW007
EUDAMED did not publish a description for this code.
CW009
The medical devices is for single use. It is intended for one patient only. Reus of a single-use devices creates a potential risk of infection for the patient or user.

Market distribution

Primary placement in Czechia; available across 2 countries total.

Country	On market since	Until
CzechiaPrimary placement	Mar 31, 2017	Mar 25, 2030
Germany	Mar 31, 2017	Mar 25, 2030

Device identification

Trade name: not provided
UDI-DI code: 18594199790174
Basic UDI-DI: 859419979REDONXH
Reference / catalog number: 99.000.22.799
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: Podtlaková lahev pro drenáž Redon, s hadicí, kulatá lahev 200 ml, operační systém, nesterilní
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 200 MU03

EMDN nomenclature code(s)

A0601010101DRAINAGE SYSTEMS WITH REDON TYPE RIGID CONTAINER

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

Certificate health across this manufacturer's portfolio.

2025-MDR/QS-024/AIssued
Quality management systemNotified body: 2265Expiry: Mar 25, 2030