PRODUCTS
MAXITEX
- Technical description
- Dimensions and Tolerances
- Guidelines for the correct use and application of the product
- Precautions, restrictions, warnings and special care
SIZE | WIDTH (mm) |
LENGTH (mm) |
SMOOTH AREA THICKNESS (MM) | AREA THICKNESS WITH TEXTURE (MM) |
6,0 | 77 ± 5mm | ≥ 260 | ≥ 0,10 | ≥ 0,13 |
6,5 | 83 ± 5mm | ≥ 260 | ≥ 0,10 | ≥ 0,13 |
7,0 | 89 ± 5mm | ≥ 270 | ≥ 0,10 | ≥ 0,13 |
7,5 | 95 ± 5mm | ≥ 270 | ≥ 0,10 | ≥ 0,13 |
8,0 | 102 ± 6 mm | ≥ 270 | ≥ 0,10 | ≥ 0,13 |
8,5 | 108 ± 6 mm | ≥ 280 | ≥ 0,10 | ≥ 0,13 |
9,0 | 114 ± 6 mm | ≥ 280 | ≥ 0,10 | ≥ 0,13 |
The MAXITEX Surgical Glove is used in invasive surgical procedures in which there is a need to protect the professional and the patient.
For correct use of the product, firstly, asepsis must be carried out with hand washing and subsequent drying, so that the gloves are then carefully put on, without rings, bracelets or others that could perforate the glove; check the appropriate size as indicated on the package.
- Contains natural latex, may cause allergy;
- There are isolated cases of allergic reactions to latex;
- If there is skin irritation, stop using the material and seek medical advice;
- Do not use if the packaging is violated;
- Single use product – never reuse the glove – destroy after use;
- Discard the glove whenever there is doubt about the contamination;
- Note the glove size before use to prevent it from tearing;
- Store in a cool, dry place at room temperature.
Classification: MAXITEX PF Surgical Gloves meet the INMETRO Ordinances 332 and 451, ABNT NBR ISO 10282 and NR6 of the MINISTRY OF LABOR.
Technical manager: Edson Pacher
CRF/SC 4300
Commercial Name: Latex Surgical Procedure Glove – Dust Free
Certificate of conformity – INMETRO: CE-LVL/ICEPEX-I 00005-33
Approval certificate – CA: 37.320
Registry ANVISA: 80748910008