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Standard Practice for Blood Irradiation Dosimetry (Withdrawn 2002)
Automatische name übersetzung:
Standard Praxis für Blutbestrahlung Dosimetrie (Withdrawn 2002)
NORM herausgegeben am 10.1.1998
Bezeichnung normen: ASTM E1939-98
Anmerkung: UNGÜLTIG
Ausgabedatum normen: 10.1.1998
SKU: NS-43663
Zahl der Seiten: 11
Gewicht ca.: 33 g (0.07 Pfund)
Land: Amerikanische technische Norm
Kategorie: Technische Normen ASTM
Keywords:
absorbed dose, absorbed-dose mapping, blood products, blood irradiation, dosimeter, dosimetry system, irradiator, ionizing radiation, measurement quality assurance plan, measurement uncertainty, radiation-sensitive indicators, reference-standard dosimeter, routine dosimeter, transfer-standard dosimeter, ICS Number Code 11.100 (Laboratory medicine), 17.240 (Radiation measurements)
1. Scope | ||||||
1.1 This practice outlines irradiator installation qualification and dosimetric procedures to be followed in the irradiation of blood and blood products by the blood-banking community. If followed, these procedures will help to ensure that the products processed with ionizing radiation from gamma, bremsstrahlung X-rays or electron sources receive absorbed doses within a predetermined range. 1.2 This practice covers dosimetry for the irradiation of blood for these types of irradiators; self-contained dry-storage 137Cs or 60Co irradiators (free-standing irradiators), teletherapy units, self-contained bremsstrahlung X-ray units and electron accelerators. The absorbed dose range for blood irradiation is typically 15 Gy to 50 Gy. 1.3 This practice also covers the use of radiation-sensitive indicators for the visual and qualitative indication that the product has been irradiated. 1.4 This practice is intended for use by technically and non-technically oriented people. It, therefore, contains more tutorial information than many other ASTM dosimetry standards. 1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. |
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2. Referenced Documents | ||||||
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