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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

6429810775HA61502C — Class I MDR by Lasinpuhaltamo T:mi…

MD Atlas
Lasinpuhaltamo T:mi Harrin Lahja ja Lasi

EUDAMED last updated this device on Dec 30, 2021

6429810775HA61502C

6429810775HA6100ZS

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Lasinpuhaltamo T:mi Harrin Lahja ja Lasi
UDI-DI code: 06429810775016
Reference / catalog number: 6429810775HA61502C

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Manufacturer information

Organization name: Lasinpuhaltamo T:mi Harrin Lahja ja Lasi
SRN: FI-MF-000018163
Manufacturer status: Active

Related devices

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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.

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: 06429810775016
Basic UDI-DI: 6429810775HA6100ZS
Reference / catalog number: 6429810775HA61502C
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: AR-Lasiputkesta (halkaisija 9mm) käsinpuhallettu korvaimukärki, jonka varsiosan pituus on 70-90 mm ja kärkiosan pituus 60mm. Imukärjen pään halkaisija on 1,5mm. Tuoteelle on myönnetty CE hyväksyntä
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L030101SUCTION AND IRRIGATION SURGICAL CANNULAS AND HANDPIECES, REUSABLE

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

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Manufacturing date
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