DEVICE: RESOLVE Systems Hb Elution Solution (06438147246120)

Device Identifier (DI) Information

RESOLVE Systems Hb Elution Solution
3024-0010
In Commercial Distribution
3024-0010
Wallac Oy
06438147246120
GS1

1
540156544 *Terms of Use
For in vitro use with the RESOLVE Hemoglobin Kits for isoelectric focusing.
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Device Characteristics

Labeling does not contain MRI Safety Information
No
No
No
No
No
Yes
No
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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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
K050709 000
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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 Record Status

e4cc329c-ddd2-449f-91c4-41de1fec490c
July 06, 2018
3
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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