Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

OLL0001072 ANE Suositus… — Class I MDD by Oy Apotti Ab

MD Atlas
Oy Apotti Ab

EUDAMED last updated this device on Feb 27, 2024

OLL0001072 ANE Suositus Postoperatiivisen pahoinvoinnin ja oksentelun riski

B-OLL0001072NC

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Oy Apotti Ab
UDI-DI code: D-OLL0001072NC
Reference / catalog number: OLL0001072 ANE Suositus Postoperatiivisen pahoinvoinnin ja oksentelun riski

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

Related devices

OLL0001052 10 metrin kävelytestiB-OLL0001052N6On the market OLL0001094 Brief psychiateric rating scale + 3B-OLL0001094NNOn the market OLL0001095 BradenB-OLL0001095NQOn the market OLL0001122 Braden QD -asteikko lasten painehaavariskin arviointiinB-OLL0001122N2On the market OLL0001096 Calgary Depression Scale for Schizophrenia B-OLL0001096NSOn the market

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-OLL0001072NC
Basic UDI-DI: B-OLL0001072NC
Reference / catalog number: OLL0001072 ANE Suositus Postoperatiivisen pahoinvoinnin ja oksentelun riski
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

Certificates

Certificate health across this manufacturer's portfolio.

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