GARDENING VELOFORTE DOC ZERO 3,5GR POWDER-FREE NITRILE GLOVES - SIZE XS (100 PCS View larger

GARDENING VELOFORTE DOC ZERO 3,5GR POWDER-FREE NITRILE GLOVES - SIZE XS (100 PCS)

ID Producto: 451

Disposable ambidextrous non-sterile nitrile glove. Totally free of talc.

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26,99 €

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Disposable ambidextrous non-sterile nitrile glove. Totally free of talc.

The micro-rough surface ensures optimal grip.
Anatomical shape with anti-roll edge.
Very sensitive and resistant.
Suitable for sensitive skin.
Suitable for hospital, outpatient and dressing use.
Recommended for use also in laboratories.
Blue color.

INFORMATION NOTE NITRILE GLOVES FOR CONTACT WITH FOOD PRODUCTS:
Suitable for short contact (contact times <30 minutes) with all aqueous (pH> 4.5), alcoholic or fatty food substances during the various processing and preparation phases, stored at room temperature and / or refrigerated with temperature not higher than 40 ° C. Wash gloves before putting them in contact with food.
The product has been subjected, where necessary, to release tests (global, specific migration), in accordance with Ministerial Decree 21/03/73 and subsequent updates, to verify the conformity of the product with current legislation on food safety. The product can therefore come into contact with food, under the intended conditions of use.

GENERAL DESCRIPTION OF THE MEDICAL DEVICE:
The product is certified as a class 1 medical device.
The gloves have also been tested to define their ability to be a waterproof barrier and offer valid protection against viral agents and potentially pathogenic microorganisms, guaranteeing the impermeability of the gloves to body and blood fluids that may contain such pests

GENERAL DESCRIPTION OF THE INDIVIDUAL PROTECTION DEVICE:
The product is certified by the Notified Body CE 0465 as PPE CLASS III for protection from MECHANICAL, CHEMICAL AND BIOLOGICAL RISKS, in accordance with the provisions of LEGISLATIVE DECREE No. 475 - implementation of Directive 89/686 / EEC Directive.

The product complies with the obligations set out in EC Regulation 1907 / 2006_REACH concerning the registration, evaluation, authorization and restriction of chemical substances and preparations within the European Union, to safeguard human health and the environment.

REFERENCE STANDARDS:
Legislative Decree no. 37/2010, EEC Directive 93/42, Directive 47/2007
Legislative Decree no. 81/2008, Consolidated Work Safety Act, Legislative Decree no. 475/92, Legislative Decree 626/94, Directive 89/686 / EEC
Italian Republic Pharmacopoeia Current Ed., European Pharmacopoeia Current Ed
EN 455 I - II - III - IV, EN 374 I - II - III, EN 420, EN 388, ASTM F1670, ASTM F1671
ISO 2859
Regulation 2023/2006 / EC and 1935/2004 / EC
Resolution ResAP (2004) on rubber products intended to come into contact with foodstuffs
Ministerial Decree 21/03/1973 and s. m. the.
DPR 777/82 and s. m. the.
EC Regulation 1907/2006 REACH

RAW MATERIALS: Synthetic Nitrile Rubber (acrylonitrile / butadiene -NBR)

The product does not contain thiurams or other chemicals believed to be toxic or harmful to human health and the environment and meets the following requirements:
- Essential requirements contained in Annex I of EC Directives 93/42 and 47/2007,
- Regulations 2023/2006 / EC and 1935/2004 / EC
- Ministerial Decree 21/03/1973 and subsequent updates and modifications
- Presidential Decree 777/82 and subsequent updates and amendments.
- Requirements of the REACH Regulation (EC 1907/2006),
- Essential requirements contained in Annex II of EC Directive 89/686.

RESIDUAL CHEMICAL PRODUCTS (additives and dyes):
ZDEC accelerators (Zinc diethyl dithiocarbamate): <0.30%
Accelerators ZDBC (zinc dibutyl dithiocarbamate): <0.30%
ZMBT accelerators (Zinc Mercaptobenzothiazole): n.d.
Antioxidant agents (Phenols, Amino derivatives, etc.): <0.80%

The presence of residues of other additives is not detectable (detection limit 0.01%).
The dyes contained in the product, where present, comply with the purity criteria of the Resolutions AP (89) document of the European Council 1 and are based on good manufacturing practices.

LUBRICANT TREATMENT:
Surface treatment by chlorination.
Amount of residual lubricating powder <2 mg / glove - according to Standard ASTM D6124 - EN ISO 21171

QUALITY CHECKS ON THE MEDICAL DEVICE:
The product complies with the essential requirements indicated in Annex I of EC Directives 93/42 and 2007/47 and with European standards EN 455-1, EN 455-2, EN 455-3, EN 455-4

GLOVE DIMENSIONS:
MIN LENGTH (mm): 240;
MIN WIDTH (mm): 80 ± 10;
MIN THICKNESS (mm):
palm: 0.07;
fingers: 0.09;
pulse: 0.05;
WEIGHT: 3.2 ± 0.3.

AQL <1.5

LATEX FREE

AVAILABLE MEASURES:
XSMALL

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