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SHIELDskin XTREME™
Sterile White Nitrile 400 DI+

Nitrile glove

To this glove in our product portfolio

Facts


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Surface cleanliness
Grip
Elongation
Endotoxin pollution
Ion-free
Cytostatics compatible
Chemical protection
sterile
textured
hand specific

Nitrile

SHIELDskin XTREME™ Sterile White Nitrile 400 DI+, Art.-No. 38244

Material: Nitrile

Properties

  • 100% nitrile
  • sterile
  • packed in pairs in foil
  • ambidextrous

Advantages

  • very good surface cleanliness
  • extra long, 40 cm
  • high abrasion resistance
  • high permeation time with disinfectants
  • tested with cytostatics

Application

  • sterile production / aseptic filling
  • for cleaning / disinfection with disinfectants and biocides
  • for the production of cytostatics
  • for heavy mechanical stress

Product recommen­dation based on cleanroom classes

Air cleanliness class EN ISO 14644-1
particulate monitored areas

123456789low dust

Hygiene zones according to GMP
microbiological monitored areas

ABCDE

PPE

Personal protective equipment
Regulation (EU) 2016/425

Cat. ICat. IICat. IIInot aplicable

A one-to-one classification of cleanroom gloves to a cleanroom class according to ISO 14644-1 is not possible. Recommendations can only be made based on cleanroom specific requirements, e.g. "abrasion resistance" or "particle emission". In the VDI guideline 2083 Part 9.2 the user can find additional information.

Technical data

    Unit of measurementValueTest method
Material     100% nitrile  
Perforation-free 1AQL value as defined in ISO 2859-1
for attribute testing on samples
  AQL1 0.65 Level 3 ISO 374-2:2019
Tear resistance before ageing
after accelerated ageing
N min./typical 6.0/10.0
6.0/8.0
EN 455-2:2015 + ASTM D412-15a
ASTM D573-04(2015)
Extreme elongation before ageing
after accelerated ageing
% min.
≥ 500
≥ 400
EN 455-2:2015 + ASTM D412-15a
ASTM D573-04(2015)
Dimensions
nominal single wall thickness
middle finger
palm
cuff
mm 0.18
0.15
0.10
ASTM D3767-03(2014)
Length   mm min./typical 400/405 EN ISO 21420:2020
Size/palm width
nominal width

6

7

8

9
10
mm 140
152
165
178
191
203
216
229
254
EN ISO 21420:2020
Extractable particles ≥ 0.5 µm fixed
typical
number/cm2
< 1,200
1,000
IEST-RP-CC005.4
Extractable substances
Ions

Ammonium (NH4+)
Bromide (Br-)
Calcium (Ca+)
Chloride (ClO2-)
Copper (Cu+)
Fluoride (F-)
Iron (Fe+)
Lithium (Li+)
Magnesium (Mg+)
Nitrate (NO3-)
Nitrite (NO2-)
Phosphate (PO43-)
Potassium (K+)
Sodium (Na+)
Sulphate (SO42-)
Zinc (Zn+)
µm/cm2
specification
0.050
0.030
0.350
0.200
n.s.
0.010
n.s.
n.s.
0.010
0.200
0.050
0.050
0.050
0.050
0.050
n.s.
µm/cm2
typical value
0.018
< 0.008
0.250
0.110
n.s.
< 0.008
n.s.
n.s.
< 0.008
0.050
< 0.008
< 0.008
0.023
0.012
0.015
n.s.
IEST-RP-CC005.4
Powder residue values   mg/gloves
typical (max.)
powder-free
≤ 1.0 (max. 2.0)
ISO 21171:2006
Chemical allergens     not detectable HPLC test method for qualitative analysis +
aqueous phosphate solution extraction
Gamma sterilized
Sterility assurance level (SAL)
    10-6 according to ANSI/ AAMI/
EN ISO 11137:2015
Silicones, amides, Di-n-octyl phthalate (DNOP)     not detectable IEST-RP-CC005.4
FTIR test procedure
Non Volatile Residues (NVR)   mg/g ≤ 30 IEST-RP-CC005.4
Endotoxins
detected by LAL test, kinetic turbidimetric
  Endotoxin units
(EU) per pair
< 20 EN 455-3:2015
Permeation resistance of medical
gloves for chemotherapeutics
    compliant ASTM D6978-05
ESD behaviour
surface resistance
contact resistance
charge decay
electrostatic properties
(construction + material requirements)
    n.s.

EN 1149-1:2006
EN 1149-2:1997
EN 1149-3:2004
EN 1149-5
PU     20 pairs
pairwise packed in PE pouch
and sealed PE bag (Peel-Pack)
 
Cardboard quantity     160 pairs
in double-walled cardboard
(8 pouch packs of 20 pairs)
 

The manufacturer's technical data listed above are typical values at the time of publication. They are not specifications. All data are without guarantee, changes are possible without prior notice.

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