BioSample collection cards make biospecimen microsampling easy and cost-effective
Ahlstrom’s BioSample collection cards are designed for micro-volume sampling, transport, and ambient storage of biological samples. Constructed of pure absorbent filters, they are free of wet strength additives and chemicals, to minimize possible interfere with reliable analytical results.
The BioSample cards are suitable for HIV viral load testing, infectious disease screening (including Hepatitis B, C, and syphilis), protein-based dried blood spot analysis, Genomics, Forensics, and human identification.
All BioSample collection cards are listed as FDA Class 1 Medical Device.
Key features of the BioSample collection cards
-
Reliable and reproducible sample collection
-
Even and uniform sample distribution
-
Customizable design and printing to meet customer need
-
Rigorous quality control and manufacturing according to ISO 13485:2016 and ISO 9001:2015
BioSample collection cards are suitable for a range of applications
- HIV viral load testing
- Infectious diseases screening including Hepatitis B, C, and Syphilis
- Protein-based dried blood spot analysis
- Genomics
- Forensics
- Human Identification
BioSample cards are available in:
- Standard format with cover for sample protection
- Simple format, without cover for easier processing
- With or without perforated circles
A drying rack is available to facilitate the drying of cards at ambient temperature.
BioSample Collection cards offering
Product |
Cards/pack |
Sample areas/
|
Max.Vol loaded/
|
Ref. Number |
Samples type |
BioSample RUO |
100 |
5 |
70 |
8.460.0001.B-N |
Blood |
BioSample RUO perforated circles | 100 | 5 | 70 | 8.460.0005.B-N | |
BioSample CE | 100 | 5 | 70 | ||
BioSample CE Barcode | 100 |
5 |
70 | ||
BioSample-CE perforated circles |
100 |
5 |
70 | ||
5 circles card RUO | 100 |
5 |
70 | ||
5 circles card-CE | 100 |
5 |
70 | ||
5 circles card-CE- perforated circles |
100 | 5 | 70 |
RUO = Research Use Only
The cards with reference number 8.460.xxxx.A are CE marked in the EU as In Vitro Diagnostic medical device in compliance with Directive 98/79/EC.
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