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COMPLIANCE INFO 1986 - 2016
Environmental Health - Public
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EHD Program Facility Records by Street Name
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2200 - Hazardous Waste Program
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PR0514003
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COMPLIANCE INFO 1986 - 2016
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Last modified
12/11/2024 9:16:23 AM
Creation date
11/6/2018 8:37:48 PM
Metadata
Fields
Template:
EHD - Public
ProgramCode
2200 - Hazardous Waste Program
File Section
COMPLIANCE INFO
FileName_PostFix
1986 - 2016
RECORD_ID
PR0514003
PE
2227
FACILITY_ID
FA0003761
FACILITY_NAME
ST JOSEPHS HOSPITAL
STREET_NUMBER
1800
Direction
N
STREET_NAME
CALIFORNIA
STREET_TYPE
ST
City
STOCKTON
Zip
95204
APN
12718044
CURRENT_STATUS
01
SITE_LOCATION
1800 N CALIFORNIA ST
P_LOCATION
01
P_DISTRICT
002
QC Status
Approved
Scanner
SJGOV\rtan
Supplemental fields
FilePath
\MIGRATIONS3\222IAError\IAError\C\CALIFORNIA\1800\PR0514003\COMPLIANCE INFO 1986 - 2016.PDF
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EHD - Public
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State of California-Health and Welfare Agenc, Department of Health Services <br /> Page 2 of 7 pages <br /> RADIOACTIVE MATERIAL LICENSE License Number: 1276-39 <br /> Amendment Number. 80 <br /> 6. Nuclide 7. Form 8. Possession Limit <br /> 2. Strontium-90 2. Sealed source 2. Total not to exceed 10 mCi. <br /> (Radiochemical Centre SIC.7) <br /> 3. Cesium-137 3. Sealed sources 3. Total 1.5 Ci, in 31 sources, no <br /> single source to exceed <br /> 65 mCi. <br /> 4. Germanium-68 4. Sealed sources (CSI Model LS *4. Each source not to exceed <br /> Series or Sanders Medical 5.5 mCi. <br /> Products Model PET series) <br /> 5. Germanium-68 5. Sealed sources(IPL Model *5. Each source not to exceed <br /> A3407 or Sanders Medical 13 mCi. <br /> Products Model PET Series) <br /> *Total possession limit for 4 <br /> and 5 not to exceed 26 mCi. <br /> 9. Authorized Use <br /> To be used for nuclear medicine procedures as specified in groups below: <br /> A. Group 1 Diagnostic studies involving measurement of uptake, dilution, or excretion but not involving <br /> imaging. <br /> Group 2 Diagnostic studies involving imaging excluding the use of Xenon-127 and/or Xenon-133 gas. <br /> Group 3 Reagent kits utilizing bulk technetium prepared by a radiopharmacy for preparation of <br /> radiopharmaceuticals listed in Group 2. <br /> Group 4 Intemal therapy and palliative treatment not usually requiring hospitalization. <br /> Group 5 Intemal therapy and palliative treatment requiring hospitalization for purposes of radiation safety. <br /> B. Group 6 Brachytherapy and Ophthalmic treatments utilizing sealed or solid sources manufactured, labeled, <br /> packaged, and distributed in accordance with a specific license issued pursuant to Title 10, Code of <br /> Federal Regulations, Part 32.74, or a specific license issued by an Agreement State or a Licensing <br /> State pursuant to equivalent state regulations (except for sources manufactured prior to <br /> August 16, 1974). <br /> L-3. Brachytherapy <br /> 4. Applicator <br /> 5. To be used in a MDS Nordion, Inc., Model GammaMed 12it HDR Afterloader for <br /> brachytherapy treatments. <br /> 6. To be used in a Cordis IRT delivery system for intravascular brachytherapy(IVB) <br /> treatments. <br />
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