21 C.F.R. § 606.60   Equipment.


Title 21 - Food and Drugs


Title 21: Food and Drugs
PART 606—CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
Subpart D—Equipment

Browse Next

§ 606.60   Equipment.

(a) Equipment used in the collection, processing, compatibility testing, storage and distribution of blood and blood components shall be maintained in a clean and orderly manner and located so as to facilitate cleaning and maintenance. The equipment shall be observed, standardized and calibrated on a regularly scheduled basis as prescribed in the Standard Operating Procedures Manual and shall perform in the manner for which it was designed so as to assure compliance with the official requirements prescribed in this chapter for blood and blood products.

(b) Equipment that shall be observed, standardized and calibrated with at least the following frequency, include but are not limited to:

 ----------------------------------------------------------------------------------------------------------------             Equipment                   Performance check            Frequency         Frequency of calibration----------------------------------------------------------------------------------------------------------------Temperature recorder..............  Compare against             Daily................  As necessary.                                     thermometer.Refrigerated centrifuge...........  Observe speed and           Each day of use......   Do.                                     temperature.Hematocrit centrifuge.............  ..........................  .....................  Standardize before                                                                                        initial use, after                                                                                        repairs or adjustments,                                                                                        and annually. Timer                                                                                        every 3 mo.General lab centrifuge............  ..........................  .....................  Tachometer every 6 mo.Automated blood-typing machine....  Observe controls for        Each day of use......                                     correct results.Hemoglobinometer..................  Standardize against         ......do.............                                     cyanmethemoglobin                                     standard.Refractometer.....................  Standardize against         ......do.............                                     distilled water.Blood container scale.............  Standardize against         ......do.............  As necessary.                                     container of known weight.Water bath........................  Observe temperature.......  ......do.............   Do.Rh view box.......................  ......do..................  ......do.............   Do.Autoclave.........................  ......do..................  Each time of use.....   Do.Serologic rotators................  Observe controls for        Each day of use......  Speed as necessary.                                     correct results.Laboratory thermometers...........  ..........................  .....................  Before initial use.Electronic thermometers...........  ..........................  .....................  Monthly.Vacuum blood agitator.............  Observe weight of the       Each day of use......  Standardize with                                     first container of blood                           container of known mass                                     filled for correct                                 or volume before initial                                     results.                                           use, and after repairs                                                                                        or adjustments.----------------------------------------------------------------------------------------------------------------

(c) Equipment employed in the sterilization of materials used in blood collection or for disposition of contaminated products shall be designed, maintained and utilized to ensure the destruction of contaminating microorganisms. The effectiveness of the sterilization procedure shall be no less than that achieved by an attained temperature of 121.5 °C (251 °F) maintained for 20 minutes by saturated steam or by an attained temperature of 170 °C (338 °F) maintained for 2 hours with dry heat.

[40 FR 53532, Nov. 18, 1975; 40 FR 55849, Dec. 2, 1975, as amended at 45 FR 9261, Feb. 12, 1980; 57 FR 11263, Apr. 2, 1992; 57 FR 12862, Apr. 13, 1992]

Browse Next






















chanrobles.com