The Code of Federal Regulations of the United States of AmericaThe Code of Federal Regulations is the codification of the general and permanent rules published in the Federal Register by the executive departments and agencies of the Federal Government. |
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1.5. rezultāts no 5.
222. lappuse
8200 Blood cell diluent . 864 . ... 2004 ) Subpart 1 _ Products Used In
Establishments That Manufacture Blood and Blood Products 864 . ... 9100 Empty
container for the collection and processing of blood and blood components . 864
.
8200 Blood cell diluent . 864 . ... 2004 ) Subpart 1 _ Products Used In
Establishments That Manufacture Blood and Blood Products 864 . ... 9100 Empty
container for the collection and processing of blood and blood components . 864
.
239. lappuse
Class II ( perform - vacuum to draw blood for subsequent ince standards ) .
reinfusion . ( b ) Classification . Class I ( general con45 FR 60637 , Sept . 12 ,
1980 ) trols ) . The manual device is exempt 864 . 8950 Russell viper venom rea
from the ...
Class II ( perform - vacuum to draw blood for subsequent ince standards ) .
reinfusion . ( b ) Classification . Class I ( general con45 FR 60637 , Sept . 12 ,
1980 ) trols ) . The manual device is exempt 864 . 8950 Russell viper venom rea
from the ...
240. lappuse
9185 Blood grouping view box . ( a ) Identification . A blood grouping view box is
a device with a glass or plastic viewing surface , which may be illuminated and
heated , that is used to view cell reactions in antigen - antibody testing .
9185 Blood grouping view box . ( a ) Identification . A blood grouping view box is
a device with a glass or plastic viewing surface , which may be illuminated and
heated , that is used to view cell reactions in antigen - antibody testing .
287. lappuse
subpart E of part 807 of this chapter Blood Gas Analyzers ; Final Guidance
subject to the limitations in 8 868 . 9 . for Industry and FDA . ' [ 47 FR 31142 , July
16 , 1982 , as amended at 61 [ 47 FR 31142 , July 16 , 1982 ; 47 FR 40410 , Sept
.
subpart E of part 807 of this chapter Blood Gas Analyzers ; Final Guidance
subject to the limitations in 8 868 . 9 . for Industry and FDA . ' [ 47 FR 31142 , July
16 , 1982 , as amended at 61 [ 47 FR 31142 , July 16 , 1982 ; 47 FR 40410 , Sept
.
322. lappuse
4330 Cardiopulmonary bypass on - line blood gas monitor . $ 870 . 4370 Roller -
type ( a ) Identification . A cardiopulmonary cardiopulmonary bypass blood
bypass on - line blood gas monitor is a pump . device used in conjunction with a
...
4330 Cardiopulmonary bypass on - line blood gas monitor . $ 870 . 4370 Roller -
type ( a ) Identification . A cardiopulmonary cardiopulmonary bypass blood
bypass on - line blood gas monitor is a pump . device used in conjunction with a
...
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accessories accordance amended amended at 65 ance standards application approval blood body caused chapter subject Class II perform Class II special Classification clinical commercial distribution completion component consists container designed determine device intended device is exempt diagnosis disease document effective electrical equipment established evaluation facility Federal files fluid Food and Drug Guidance hearing human Identification implanted indicate joint July 25 June labeling limitations manufacturer material means measure ment monitor notice operation paragraph patient person placed powered practice premarket notification procedures pressure procedures in subpart prosthesis reagents reasonable records regulation request respect Sept serum special controls specific statement submit subpart E surgical test system tion tissue treatment trols tube unit unless vice x-ray
Populāri fragmenti
11. lappuse - Insufficiency of label space for the prominent placing of such word, statement, or information, resulting from the use of label space for any word, statement, design, or device which is not required by or under authority of the act to appear on the label; (5) Insufficiency of label space for the...
18. lappuse - Act (1) small open containers of fresh fruits and fresh vegetables and (2) food which is, in accordance with the practice of the trade, to be processed, labeled, or repacked in substantial quantities at establishments other than those where originally processed or packed, on condition that such food is not adulterated or misbranded under the provisions of this Act upon removal from such processing, labeling, or repacking establishment.
356. lappuse - Act. (b) References in this part to regulatory sections of the Code of Federal Regulations are to Chapter I of Title 21, unless otherwise noted.
86. lappuse - In computing any period of time prescribed or allowed by this part, the day of the act, event, or default after which the designated period of time begins to run is not to be included. The last day of the period so computed is to be included, unless it is...
79. lappuse - label" means a display of written, printed, or graphic matter upon the immediate container of any substance; and a requirement made by or under authority of this Act that any word, statement, or other information appear on the label shall not be considered to be complied with unless such word, statement, or other information also appears...
578. lappuse - Nothing in this section shall authorize the withholding of information by the Secretary or any officer or employee under his control, from the duly authorized committees of the Congress.
15. lappuse - On packages containing 4 pounds or 1 gallon or more and labeled in terms of weight or fluid measure, the declaration shall be expressed in pounds for weight units with any remainder in terms of ounces or common or decimal fractions of the pound; in the case of fluid measure, it shall be expressed in the largest whole unit...
15. lappuse - 6 oz net wt.," and "6 fl oz" or "net contents 6 fl oz". (j) On packages containing 4 pounds or 1 gallon or more and labeled in terms of weight or fluid measure, the declaration shall be expressed in pounds for weight units with any remainder in terms of ounces or common or decimal fractions of the pound...
56. lappuse - (1) the term 'manufacture, preparation, propagation, compounding, or processing' shall include repackaging or otherwise changing the container, wrapper, or labeling of any drug package in furtherance of the distribution of the drug from the original place of manufacture to the person who makes final delivery or sale to the ultimate consumer; "(2) the term 'name...
Bibliogrāfiskā informācija
| Nosaukums | The Code of Federal Regulations of the United States of America |
| Atbalstītāji | United States. Division of the Federal Register, United States. Federal Register Division, United States. Office of the Federal Register |
| Izdevējs | U.S. Government Printing Office, 2006 |
| ISBN | 0160758246, 9780160758249 |
| Eksportēt avotu | BiBTeX EndNote RefMan |