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

3540110 — Class I MDR by Lasinpuhaltamo Hakola Oy

MD Atlas
Lasinpuhaltamo Hakola Oy

EUDAMED last updated this device on Dec 13, 2021

3540110

643005864354011099

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Lasinpuhaltamo Hakola Oy
UDI-DI code: 06430058640424
Reference / catalog number: 3540110

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: Lasinpuhaltamo Hakola Oy
SRN: FI-MF-000012479
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
Puhdistus/sterilointi ja tarkastus ennen käyttöä.

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: 06430058640424
Basic UDI-DI: 643005864354011099
Reference / catalog number: 3540110
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Lasinen imukärki on tarkoitettu käytettäväksi ihmisen luonnollisiin aukkoihin, kuten nenään ja korvaan, kohdistuviin toimenpiteisiin.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: Imukärki 3,5-4,0 x 110 mm

EMDN nomenclature code(s)

Q0399ENT 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

Related devices

20706430058642070WCOn the market 202555643005864202555CKOn the market 3011064300586430110KNOn the market 1010064300586410100JVOn the market 1011064300586410110JYOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.