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.
292. lappuse
2610 Gas pressure gauge . monitor relative changes in a hemodynamically
stable patient ' s cu( a ) Identification . A gas pressure taneous carbon dioxide
tension as an gauge ( e . g . , bourdon tube pressure adjunct to arterial carbon
dioxide ...
2610 Gas pressure gauge . monitor relative changes in a hemodynamically
stable patient ' s cu( a ) Identification . A gas pressure taneous carbon dioxide
tension as an gauge ( e . g . , bourdon tube pressure adjunct to arterial carbon
dioxide ...
293. lappuse
A gas pressure calibrator is a device intended for medical purposes that is used
to calibrate pressure - measuring instruments by generating a known gas
pressure . ( b ) Classification . Class I ( general controls ) . The device is exempt
from the ...
A gas pressure calibrator is a device intended for medical purposes that is used
to calibrate pressure - measuring instruments by generating a known gas
pressure . ( b ) Classification . Class I ( general controls ) . The device is exempt
from the ...
302. lappuse
Pressure tubing and accessories are flexible or rigid devices intended to deliver
pressurized medical gases . ( b ) Classification . Class I ( general controls ) . The
device is exempt from the premarket notification procedures in subpart E of part ...
Pressure tubing and accessories are flexible or rigid devices intended to deliver
pressurized medical gases . ( b ) Classification . Class I ( general controls ) . The
device is exempt from the premarket notification procedures in subpart E of part ...
308. lappuse
A venous bloot pressure manometer is a device attached to a venous catheter to
indicate manometrically the central or peripheral venous pressure . ( b )
Classification . Class II ( performance standards ) . 8870 . 1025 Arrhythmia
detector and ...
A venous bloot pressure manometer is a device attached to a venous catheter to
indicate manometrically the central or peripheral venous pressure . ( b )
Classification . Class II ( performance standards ) . 8870 . 1025 Arrhythmia
detector and ...
314. lappuse
An extravascular blood pressure transducer is a device used to measure blood
pressure by changes in the mechanical or electrical properties of the device . The
proximal end of the transducer is connected to a pressure monitor that produces
...
An extravascular blood pressure transducer is a device used to measure blood
pressure by changes in the mechanical or electrical properties of the device . The
proximal end of the transducer is connected to a pressure monitor that produces
...
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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 |