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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

OLL0001078 PÄIV LAPSEN SEPSIS… — Class I MDD by Oy Apotti Ab

MD Atlas
Oy Apotti Ab

EUDAMED last updated this device on Feb 27, 2024

OLL0001078 PÄIV LAPSEN SEPSIS PÄIVYSTYSHOIDON AIKANA

B-OLL0001078NQ

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Oy Apotti Ab
UDI-DI code: D-OLL0001078NQ
Reference / catalog number: OLL0001078 PÄIV LAPSEN SEPSIS PÄIVYSTYSHOIDON AIKANA

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Manufacturer information

Organization name: Oy Apotti Ab
SRN: FI-MF-000007544
Manufacturer status: Active

Market distribution

Primary placement in Finland; available across 1 country total.

Placed on the market in Finland; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: D-OLL0001078NQ
Basic UDI-DI: B-OLL0001078NQ
Reference / catalog number: OLL0001078 PÄIV LAPSEN SEPSIS PÄIVYSTYSHOIDON AIKANA
Issuing entity: EUDAMED

Classification

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

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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

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Certificates

Certificate health across this manufacturer's portfolio.

FI25/00000062Issued
Quality management systemNotified body: 0598Expiry: Oct 23, 2028