DEVICE: RESOLVE Systems Hemoglobin Kit (06438147000784)

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Device Identifier (DI) Information

RESOLVE Systems Hemoglobin Kit
FR-9120
FR-9120
Wallac Oy
06438147000784
GS1
1
For detection of normal and variant hemoglobins.
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Device Characteristics

Labeling does not contain MRI Safety Information
No
No
No
No
No
Yes
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No

GMDN

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GMDN Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.

GMDN Preferred Term Name GMDN Definition
Multiple haemoglogbin subtype IVD, kit, electrophoresis A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative determination of one or multiple subtypes of haemoglobin in a clinical specimen, using an electrophoresis method.
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FDA Product Code

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Product Code Product Code Name
GKA Abnormal Hemoglobin Quantitation
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Sterilization

No
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

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Storage and Handling
Storage Environment Temperature: between 2 and 8 Degrees Celsius
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Clinically Relevant Size

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Size Type Text
No Device Sizes
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Device Status

In Commercial Distribution
February 02, 2016

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Alternative and Additional Identifiers Additional Identifiers

Package DI

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Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
No Package DIs found
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Secondary DI

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Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

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Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

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No
No
None
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Production Identifier(s) in UDI

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Yes
No
Yes
No
No CLOSE

Customer Contact

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No Customer Contact currently defined
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