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Brochure Sogetub Pour Sifa 2019 - Decembre 2019 - (2) - 6

The document discusses MEDICALFEIN copper tube which complies with EU medical device directives and standards for use in medical gas systems. The tube has a very low carbon residue inner surface which protects against corrosion and reduces the risk of fire and gas contamination.

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0% found this document useful (0 votes)
70 views1 page

Brochure Sogetub Pour Sifa 2019 - Decembre 2019 - (2) - 6

The document discusses MEDICALFEIN copper tube which complies with EU medical device directives and standards for use in medical gas systems. The tube has a very low carbon residue inner surface which protects against corrosion and reduces the risk of fire and gas contamination.

Uploaded by

Tâm Tâm
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Medical

MEDICAL
Medical
Fein
FEIN
Fein
MEDICALFEIN copper tube complies with
the requirements of Directive 93/42/
EEC and subsequent amendments and it is
classified as a CLASS IIA medical device. It
is intended to be used in the manufacture of
medical gas, medical gas mixtures, air and
vacuum pipeline systems, and of anesthetic
Medical Fein
gases scavenging systems, according to the
relevant standards. Every lot is released with
Medical Fein the issue of an EN 10204 ref. 3.1 quality
certificate,
MEDICALFEIN in order
copper to tube
assess the conformity
complies with standard. S
of the tube to the requirements
the requirements of Directive 93/42/ of EN 13348 is an harmo
EEC and standard.
subsequent Sinceamendments
the standardand EN it13348
is Directive, th
MEDICALFEIN copper tube complies with standard.
classified is anas harmonized
Since a CLASS IIAstandard
the standard EN 13348 for the PED
medical device. It consequen
the requirements of Directive 93/42/ is an harmonized
Directive,
is intended bestandard
tothe MEDICALFEIN
used in the for manufacture
thetube
PED complies of Directive to
EEC and subsequent amendments and it is Directive,
medical the
gas,MEDICALFEIN
consequentlymedical to gas tube complies
mixtures,
the requirements air and
of this in the inner
classified as a CLASS IIA medical device. It consequently
vacuum to the requirements
Directive too. The very low of
pipeline systems, and ofanesthetic
this residue
carbon copper tub
is intended to be used in the manufacture of Directive too. The very
gasesinscavenging low carbon
systems, residue
EN 13348 with qualification the inner surface ofaccording
the MEDICALFEINto the against cor
medical gas, medical gas mixtures, air and in relevant
the innerstandards.
surface of Every the MEDICALFEIN
lot is released with and gas co
assessment for the materials copper tube guarantees the protection
vacuum pipeline systems, and of anesthetic copper tube
the issue ofguarantees
an EN 10204 the protection
ref. 3.1 quality
conforminggases
to ENscavenging
10204 requirements.
systems, according to the against
against corrosion
corrosion and reduces
andtoreduces the risk of fire
certificate, in order assess the risk of fire
conformity
DHP copperrelevant
tube (Cu+Ag min.
standards. 99.90%;
Every lot is released with and and gas contamination.
of gas contamination.
the tube to the requirements of EN 13348 EN 13348
0.015%≤P≤0.040%) available
the issue of an EN 10204 in soft
ref. 3.1 quality assessme
50 m coilscertificate,
or hard and half hard
in order 5 mthe conformity
to assess conformi
straight lengths, bearing
of the tube to theCE marking of EN 13348
requirements EN 13348 with qualification
according to Directive 93/42/EEC assessment for the materials DHP copp
and following amendments given by conforming to EN 10204 requirements. 0.015%
50 m coi
Directive 2007/47/EC . DHP copper tube (Cu+Ag min. 99.90%; straight l
0.015%P0.040%) available in soft according
50 m coils or hard and half hard 5 m and follo
straight lengths, bearing CE marking Directive
according to Directive 93/42/EEC
6 and following amendments given by
Directive 2007/47/EC .
6

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