DEVICE: DiaSpect Hemoglobin Cuvettes (04048534001540)
Device Identifier (DI) Information
DiaSpect Hemoglobin Cuvettes
90C.0001
In Commercial Distribution
DiaSpect Medical GmbH
90C.0001
In Commercial Distribution
DiaSpect Medical GmbH
For the quantitative determination of hemoglobin in whole blood.
Device Characteristics
Labeling does not contain MRI Safety Information | |
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No | |
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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? |
---|---|---|---|---|
32435 | Haemoglobin analyser IVD, point-of-care |
A mains electricity (AC-powered) instrument, which may include internal rechargeable batteries, intended to be used by health professionals at the point-of-care, and often also in the laboratory, to determine the concentration of haemoglobin in a clinical specimen, using technology which may include colorimetry, electrometry or photometry.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
GKR | System, Hemoglobin, Automated |
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 0 and 50 Degrees Celsius |
Special Storage Condition, Specify: Temperatures of -30°C up to +70°C temporarily permitted during transport (24 hrs max.) |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
01ddda57-38cb-4ba7-b845-cb0bb94e2c6b
December 28, 2022
1
December 20, 2022
December 28, 2022
1
December 20, 2022
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
04048534001694 | 5 | 04048534001540 | In Commercial Distribution | cardboard box |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
04048534001687
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+4939203511414
support@ekf-diagnostic.de 1-800-531-5535
techsupport@ekfdiagnostics.com
support@ekf-diagnostic.de 1-800-531-5535
techsupport@ekfdiagnostics.com