GRANBERG 111.220 Disposable Examination and Protective Gloves User Manual

111.220
111.325

111.220 Disposable Examination and Protective Gloves

PRODUCT-SPECIFIC INFORMATION ON THIS PAGE ONLY
111.220 Disposable Examination and Protective Gloves Granberg. Vinyl, non- sterile, powder-free, phthalates-free.
Clear colour.

Available
sizes| XS| S| M| L| XL
---|---|---|---|---|---
5/6| 6/7| 7/8| 8/9| 9/10

111.325 Disposable Examination and Protective Gloves Granberg. Vinyl, non- sterile, powder-free.
Blue colour.

Available
sizes| S| M| L| XL
---|---|---|---|---
6/7| 7/8| 8/9| 9/10

EN ISO 21420:2020

EN ISO 374-1:2016+A1:2018
(Type B)| Permeation
Performance Level| Measured Breakthrough
Time (minutes)| EN ISO 374-4:2019
Mean Degradation (%)
---|---|---|---
K| 40% Sodium Hydroxide| 6| > 480| -33.
P| 30% Hydrogen Peroxide| 6| > 480| -18.
T| 37% Formaldehyde| 6| > 480| –16.0

USER MANUAL FOR DISPOSABLE GLOVES CATEGORY III and MEDICAL DEVICE

The User Manual should be used with product-specific information.
User Instructions should be read before using.

INTENDED USE

Powder-free examination and protective disposable vinyl gloves are intended for use in the medical field to protect patients and users from cross- contamination. These gloves are also intended to protect against certain chemicals, microorganisms where hand protection is needed.
Foodstuff-approved gloves are marked with relevant food pictograms and comply with relevant EU Regulations. Gloves should be used only according to their intended purpose.

WARNINGS AND PRECAUTIONS OF USE

This information does not reflect the actual duration of protection in the workplace and the differentiation between mixtures and pure chemicals and other factors influencing the performance such as temperature, abrasion, degradation etc. The chemical resistance has been assessed under laboratory conditions from samples taken from the palm only (except in cases where the glove is equal to or over 400 mm – where the cuff is tested also) and relates only to the chemical tested. It can be different if the  chemicals used in a mixture. It is recommended to check that the gloves are suitable for the intended use because the conditions at the workplace may differ from the type test depending on temperature, abrasion, and degradation. When used, protective gloves may provide less resistance to a dangerous chemical due to changes in physical properties. Movements, snagging, rubbing, degradation caused by chemical contact, etc., may reduce the actual use time significantly. For corrosive chemicals, degradation can be the most important factor to consider in the selection of chemical-resistant gloves. Degradation levels (EN ISO 374-4:2019) indicate the change in puncture resistance of the gloves after exposure to the challenge chemical. The penetration resistance has been assessed under laboratory conditions and relates only to the tested specimens.

PRODUCT INSTRUCTION FOR USE

Before use, after donning, and during use inspect the gloves for any defect or imperfections and discontinue use immediately if signs of tearing, swelling or degradation, or any damage appear. Dry hand before donning. Ensure chemicals or residuals cannot enter through the cuff. Change glove after each patient. Always select the correct size glove for your hand. For donning, hold the glove by the bead with one hand. Align the glove thumb with your other hand thumb and slide your hand into the glove, one finger into each glove finger. Pull by the glove palm to get a good fit. Don the other glove by the same procedure. Doffing, hold glove bead and pull toward the finger until the glove come off. For Single Use only. If re-used, the risk of contamination and infection increases due to improper cleaning processes; and increased risk of holes and tear during re-use due to weakening of gloves by cleaning processes. Poorly-fitting gloves will greatly reduce dexterity and cause fatigue. Using the wrong glove size leads to inadequate hand protection. When an indication for hand hygiene precedes a contact that also requires glove usage, hand rubbing or hand washing should be performed before donning gloves and after removing gloves.

DISPOSAL

Used gloves can be contaminated and must be disposed of under hospital policy and/or local regulation.

INGREDIENTS/HAZARDOUS COMPONENTS

Components used in glove manufacturing may cause allergic reactions in some users. If allergic reactions occur, seek medical advice immediately. Where relevant, a list of substances contained in the glove that are known to cause allergies, per listed in Annex G of EN ISO 21420:2020, shall be supplied on request.

STORAGE

Store in a cool and dry place in its original package. Opened boxes should be kept away from fluorescent and sunlight. Keep the gloves away from ozone, heating devices, and the source of the fire. Gloves are packed in a dispenser box suitable for transport. Keep the gloves in the box when not in use. The shelf life for products stored as recommended is mentioned on each package. Service life cannot be specified and depends on the application and responsibility of the user to determine the suitability of the glove for its intended use.

REPORTING OF INCIDENTS

In case of any serious incident occurred with the use of this device, please report it to the manufacturer
and the competent Authority.
Further information can be obtained from the manufacturer, please contact Granberg AS.

EXPLANATION OF SYMBOLS AND PICTOGRAMS USED

Protective gloves against dangerous chemicals and microorganisms – Part 1: Terminology and performance requirements for chemical risks. EN ISO 374-1:2016+A1:2018. Definition of breakthrough time through the glove palm (1 µg/cm2/min).
Type A > level 2 for 6 chemicals, Type B > level 2 for 3 chemicals, Type C > level 1 for 1 chemical (no code under pictogram).

*Indicates that the glove falls below the minimum performance level as stated in EN ISO 374-1:2016+A1:2018 for the given individual hazard.

Add tional information on chemical resistance obtainable from manufacturer.

| Protection against bacteria, fungi and viruses
---|---
| Protection against bacteria and fungi, not tested against viruses
| Suitable for contact with foodstuffs.
Note: not all gloves that are suitable for handling food may be suitable for all types of food. Check the
Food Declaration of Compliance.
| Manufacturer
| Date of manufacture
| Expiry date
| Lot number
| Fragile, handle with care
| Keep away from sunlight
| Keep dry
| Temperature limit
| Do not reuse
| Check User Instruction
| Caution
| Non-sterile
| Raw material latex
| Do not contain natural rubber
| Corrugated cardboard
| Non-corrugated paperboard
| Paper
| Medical Device
| Unique Device Identifier
| Article number

Latex free: yes.
This product is Category III Personal Protective Equipment as per Regulation (EU) 2016/425 and complies with standards: EN ISO 21420:2020, EN ISO 374-1:2016+A1:2018, EN ISO 374-4:2019, EN ISO 374-5:2016.
EU Declaration of Conformity: www.granberg.no/search
Notified Body responsible for EU Type Examination and ongoing conformity: SATRA Technology Europe Ltd. (NB No. 2777), Bracetown Business Park, Clonee, D15YN2P, Republic of Ireland.
This product is classified as Class I Medical Device according to Annex VIII of the Regulation (EU) 2017/745 and complies with standards: EN 455-1, EN 455-2, EN 455-3, EN 455-4, ISO 15223-1:2021.

Head office: GRANBERG AS,
Bjoavegen 1442, 5584 Bjoa, Norway.
Phone: +47 53 77 53 00
E-mail: post@granberg.no
Swedish office: GRANBERG SVERIGE AB,
Schubergsvägen 20, 311 74 Falkenberg, Sweden.
Phone: +46 (0)346 124 25
E-mail: post@granberg-ab.se
User Manual issue date: 06.02.2024
granberggloves.com

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