9542

Organization name

HTL-Strefa S.A.

SRN

PL-MF-000002198

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

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

• CW010

  EUDAMED did not publish a description for this code.
• CW262

  EUDAMED did not publish a description for this code.

Primary placement in Hungary; available across 1 country total.

Trade name

not provided

UDI-DI code

05903999608279

Basic UDI-DI

590799609710ML

Reference / catalog number

9542

Issuing entity

GS1

Risk category

Class I

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

Lancing device is a medical device for multiple use with sterile, single-use lancets intended for capillary blood sampling by a lay person."

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER