santex powdered

Organization name

Mercator Medical Spółka Akcyjna

SRN

PL-MF-000018942

Manufacturer status

Active

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

• CW999

  This product is intended for single use. Do not reuse. Do not use if the packaging has been damaged. Do not use after the expiry date stated on the package label. Do not use if labelling is incomplete or illegible. Components used in gloves production process may cause allergic reactions in some people. Some gloves may contain components known to be a possible cause of allergy for person allergic to them, who may develop contact irritation and/or allergic reaction. In case of an allergic reaction consult a doctor.

Primary placement in Poland; available across 26 countries total.

Trade name

santex powdered

UDI-DI code

05906615011798

Basic UDI-DI

5906615RDNSLPP9N

Reference / catalog number

RD11257002_1573

Issuing entity

GS1

Risk category

Class I

Applicable legislation

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

Status

On the market

Quantity

100

Additional product description

S

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.

• T010201LATEX EXAMINATION / TREATMENT GLOVES