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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

150012 — Class III MDR by Contipro a.s.

MD Atlas
Contipro a.s.

EUDAMED last updated this device on Mar 25, 2026

150012

859516377700N8

On the marketClass III

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Contipro a.s.
UDI-DI code: 08595163777019
Reference / catalog number: 150012

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Manufacturer information

Organization name: Contipro a.s.
SRN: CZ-MF-000014702
Manufacturer status: Active

Related devices

160017859516379900NYOn the market N/AB-Hyatoprol22SAOn the market N/AB-Hyatoprol50SFOn the market N/AB-Hyio227MOn the market N/AB-HyioYSOn the market

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW264
Octenidine dihydrochloride
CW007
EUDAMED did not publish a description for this code.
CW030
For professional use only.

Market distribution

Primary placement in Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement	Oct 12, 2023	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08595163777019
Basic UDI-DI: 859516377700N8
Reference / catalog number: 150012
Issuing entity: GS1

Classification

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

Device details

Quantity: 6
Additional product description: Sicalm HA je sterilní zdravotnický prostředek určený k mechanické ochraně a hojení traumatizované tkáně v dutině ústní.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q010399SURGICAL DENTAL 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

Certificate health across this manufacturer's portfolio.

2025-MDR/TD-033Issued
Technical documentationNotified body: 2265Expiry: Aug 4, 2028
2025-MDR/QS-033Issued
Quality management systemNotified body: 2265Expiry: Aug 4, 2028
2023-MDR/TD-016Issued
Technical documentationNotified body: 2265Expiry: Aug 4, 2028
2023-MDR/QS-016Issued
Quality management systemNotified body: 2265Expiry: Aug 4, 2028