DEVICE: DiaSpect Hemoglobin Cuvettes (04048534001540)

Device Identifier (DI) Information

DiaSpect Hemoglobin Cuvettes
90C.0001
In Commercial Distribution

DiaSpect Medical GmbH
04048534001540
GS1

100
341050309 *Terms of Use
For the quantitative determination of hemoglobin in whole blood.
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Device Characteristics

Labeling does not contain MRI Safety Information
No
No
Yes
Yes
No
No
No
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.
Active false
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FDA Product Code

[?]
Product Code Product Code Name
GKR System, Hemoglobin, Automated
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
Premarket Submission Number Not Available/Not Released
No CLOSE

Sterilization

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

[?]
Storage and Handling
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.)
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Clinically Relevant Size

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Size Type Text
No Device Sizes
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Device Record Status

01ddda57-38cb-4ba7-b845-cb0bb94e2c6b
December 28, 2022
1
December 20, 2022
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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
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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

[?]
Unit of Use DI Number: 04048534001687 CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
Yes
No
No CLOSE

Customer Contact

[?]
+4939203511414
support@ekf-diagnostic.de
1-800-531-5535
techsupport@ekfdiagnostics.com
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