ГОСТ Р ИСО 1135-5—2022
Библиография
[1]ISO 291, Plastics — Standard atmospheres for conditioning and testing
[2]ISO 7000, Graphical symbols for use on equipment — Registered symbols
[3] ISO 11135, Sterilization of health-care products — Ethylene oxide — Requirements for the development, validation
and routine control of a sterilization process for medical devices
[4] ISO 11137 (all parts), Sterilization of health care products — Requirements for validation and routine control —
Radiation sterilization
[5] ISO 17665-1, Sterilization of health care products — Moist heat — Part 1: Requirements for the development, val
idation and routine control of a sterilization process for medical devices
[6] IEC 80416-1, Basic principles for graphical symbols for use on equipment — Part 1: Creation of graphical symbols
for registration
[7]European Pharmacopoeia
[8]United States Pharmacopeia
[9]Japanese Pharmacopoeia
[10] Nightingale M.J. Improving compatibility between blood packs and transfusion sets. Transfus. Med. 2006, 16
pp. 11—15
[11] Nightingale M.J., & Leimbach R. An evaluation of proposed changes to International Standards for blood bags and
transfusion sets to improve their compatibility. Transfus. Med. 2008, 18 pp. 281—286
[12] Nightingale M.J., Norfolk D.R., Pinchon D.J. The current uses of transfusion administration sets — a cause for
concern? Transfus. Med. 2010, 20 pp. 291—302
[13] EN 15986, Symbol for use in the labelling of medical devices — Requirements of medical devices containing
phthalates
[14] Bashir S., Nightingale M.J., Cardigan R. Ensuring that blood transfusion sets administer an effective dose of func
tional blood components. Transfus. Med. 2013, 23 pp. 226—230
[15]ISO 7864, Sterile hypodermic needles for single use
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