Latex Gloves with Aloe Vera Reflexx Care L600 – g. 6.2 (M)

  • ALOE VERA is processed in the inner side of the glove in a cold cycle without using grease. It is then dried to preserve all the features, without affecting the beneficial properties of the plant. The heat and humidity of the hand reactivate the beneficial properties of ALOE VERA.
  • Micro roughened surface for increased grip and sensitiveness.
  • Powder free to reduce dermatitis and contamination risks.
  • Inner chlorination for easier donning.
  • Silicon not present in the gloves’ composition.

Overview

  • PPE Cat. 3 for safety from chemichal components and micro-organism risks (Reg. EU 2016/425).
    • EN ISO 374-1:2016 / TYPE C: certified with one chemical.
    • EN ISO 374-5:2016 / VIRUS: for protection against bacteria, fungi and VIRUS.
  • MEDICAL DEVICE, to be used as an examination glove in medical and dental field (AQL 1.5), also invasively, intended for temporary use (according to Reg EU 2017/745, EN 455 1, 2, 3 & 4 norms).

Features

Material: Latex
Color: Green
External surface: Microroughened
Inner surface: Powder free
Chlorination: Inner
AQL: ≤ 1,5
Length - cm: 24
Thickness - mm: 0,12
Weight - g. size M: 6,20

Recommended for

Dental

Medical

Surface: Textured

Length: 24 cm

Thickness: 0,12 mm +/-0,03

Weight: 6.20 g +/-0,3 (size M)

Colour: Green

Other features: Inner chlorination

SIZES AND PACKAGING: XS – S – M – L – XL

PACK 100

CART. 10×100

CODES EAN DISPENSER EAN CARTON BOX
L600/XS 8032891632130 8032891637135
L600/S 8032891632147 8032891637142
L600/M 8032891632154 8032891637159
L600/L 8032891632161 8032891637166
L600/XL 8032891632178 8032891637173

The CE marking (European Conformity marking) attests that the product meets the European Union rules and requirements for manufacturing and commercial marketing.

Products usable as Medical Devices according to Reg EU 2017/745, EN 455 1, 2, 3 & 4 norms. The Reg EU 2017/745 on medical devices provides the requirements for the production of gloves to be used in health (and therefore also dental), as well as the obligations of labeling and assessment of biological safety. The gloves considered Medical Devices provide protection from cross-contamination both for the patient and the user as they are considered an effective barrier to biological fluids and microorganisms.

In April 2018 the New PPE Regulation EU 2016/425 has amended and replaced the previous PPE Directive 89/686/EEC. The new PPE regulation now specifies three classes based on risk definitions:

– CAT I: minimal risk, self-certified;

– CAT II: intermediate risks (other than those listed in Categories I and III), certified by approved body;

– CAT III: very serious risks, which may cause death or irreversible damage to health; certified by approved body.

Only the approved bodies may issue a CE mark for PPE CAT II and CAT III. Without a proper CE mark the gloves may not be sold or used.

Disposal

Disposable Gloves

Material: latex

Garbage Can: general waste

Always check the disposal rules of your municipality

Primary Packaging (Dispenser)

Item: non corrugated cardboard box.

Material: paper PAP 21

Garbage Can: recycling bin

Always check the disposal rules of your municipality

Secondary Packaging (Carton Box)

Item: corrugated cardboard box.

Material: paper PAP 20

Garbage Can: recycling bin

Always check the disposal rules of your municipality

Empty the packaging of its contents before collecting it. Reduce the volume of the dispenser and box.

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Contact us
For any need regarding the production, distribution and sale of our disposable gloves in latex, nitrile, polyethylene, vinyl and reusable, do not hesitate to contact us: we will be at your disposal with competence and professionalism.
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