Compresses nonsterile 10x8 16 plys. a100

Organization name

Lola Ribar d.o.o. za proizvodnju saniteta

SRN

HR-MF-000018260

Manufacturer status

Active

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

• CW999

  Non-sterile product intended for external wounds. Must be sterilised before use. Product is not to be used if the packaging is damaged or the product is visibly unclean. The appropriate packaging for the sterilisation process and the cleanliness of the product during the preparation for sterilisation are to be provided by the healthcare institution. The process of product packaging and its sterilisation are to be carried out using validated methods.Single use only. Do not reuse. Once sterilised, do not resterilise. The edges of the prepared products must be free of loose threads during use. Visible damage to the gauze weave – do not use. Comply with the mandatory hospital procedures of counting medical products before and after use. Do not use after the expiration date. Comply with the mandatory procedures for the disposal of used medical products in accordance with the national laws

Primary placement in Croatia; available across 1 country total.

Trade name

Compresses nonsterile 10x8 16 plys. a100

UDI-DI code

03858890790672

Basic UDI-DI

3858890791NESTLR

Reference / catalog number

7200

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

Sales unit consists of 100 pieces. Hydrophilic white gauze, chemically neutral, cut and folded in various sizes and layers. Sterilisation required before use. Compresses are intended for absorbing blood and secretions. Pre-sterilised, used during surgery and the dressing of postoperative wounds. Also used to treat a wide range of external and superficial wounds.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• ±0,5cm

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

• M0201020102COTTON GAUZES, FOLDED, WITHOUT X-RAY DETECTABLE THREAD, NON-STERILE