DEVICE: Precision Xceed Pro (00357599000189)
Device Identifier (DI) Information
Precision Xceed Pro
70907-03
In Commercial Distribution
70907-03
ABBOTT DIABETES CARE INC
70907-03
In Commercial Distribution
70907-03
ABBOTT DIABETES CARE INC
Precision Xceed Pro Blood Glucose and ?-Ketone Monitoring System
Device Characteristics
Labeling does not contain MRI Safety Information | |
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No | |
No | |
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No | |
Yes | |
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No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
62643 | Multiple clinical chemistry analyte monitoring system IVD, home-use |
A collection of devices including a portable, electrically-powered, semi-automated or automated instrument (self-testing meter), reagents, test strips and/or other associated materials and accessories (e.g., control solutions, lancets) intended to be used together for the quantitative measurement of multiple clinical chemistry analytes in a clinical specimen. Analytes detected may include electrolytes, specific proteins, clinical chemistry substrates (e.g., lipid profile), liver and/or cardiac function test analytes, and/or enzymes. It is intended to be used for self-testing by a layperson in the home, and some types may in addition be used at the point-of-care.
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Active | false |
62644 | Multiple clinical chemistry analyte monitoring system IVD, point-of-care |
A collection of devices that includes one or more portable, electrically-powered instruments (meter), reagents, test strips and/or other associated materials and accessories [e.g., control solutions, lancets] intended to be used together exclusively at the point-of-care by medical professionals for the quantitative measurement of more than one clinical chemistry analyte [e.g., glucose, ketones, lipid(s), and/or creatinine] in a whole blood specimen. Some types may also include measurement of haemoglobin and/or haematocrit for rapid diagnosis of anaemia and/or blood loss.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
LFR | Glucose dehydrogenase, glucose |
NBW | SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER |
JIN | NITROPRUSSIDE, KETONES (URINARY, NON-QUANT.) |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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Storage Environment Temperature: between -4 and 122 Degrees Fahrenheit |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
76fc003a-8a87-49a3-b347-ba8649271226
April 18, 2024
9
August 12, 2016
April 18, 2024
9
August 12, 2016
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
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No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+1(877)529-7185
xx@xx.xx
xx@xx.xx