The BD Microtainer® MAP Microtube for Automated Process is the first one–piece, instrument–compatible microtube to offer both standard full–size patient identification labels as well as compatibility with most automated haematology instruments.
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BD Microtainer® MAP Microtube for Automated Process
Automate processing with the first one-piece, instrument–compatible microtube
- Overview
- EIFU & Resources
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Automated processing
The microtube streamlines operations by allowing the automated processing of your microcollection haematology samples.
Safety
It enhances patient safety by accommodating full-size patient identification labels at the time of collection.
Improved workflow
It improves workflow with a one-piece design, without parts to assemble and without contaminated parts to discard.
Testing
It is approved for haematology testing.
Twist-assist closure
Easy to open with twist-locking mechanism that ensures no leakage.
Pierceable cap
Compatible with main haematology analysers without the need for a tube adapter.
One piece
A capillary blood tube with standard blood collection tube dimensions (13 x 75 mm) and penetrable closure.
Visible fill lines
Three clearly visible fill markings ensure the correct sample volume (250-500 μl).
Identification
A standard label can be attached directly to the sample, minimising the risk of misidentification due to missing or incomplete labelling.
Colour marking
Colour marking for identification of the type of sample.
Literature
BD's collection of literature on industry and on our offerings gives you information you can use to continue striving for excellence.
Learn more
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Please note, not all products, services or features of products and services may be available in your local area. Please check with your local BD representative.
The Microtainer® Blood Collection Tubes are in vitro diagnostic medical devices and are CE marked in compliance with the European In Vitro Diagnostic Medical Device Directive 98/79/EC
The lancets are medical devices, they are CE marked in compliance with European Medical Device Directive 93/42/EEC and are CE certified by NSAI - National Standards Authority of Ireland (Notified Body Number = 0050)
BD-18635
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