The report also covers details on the market’s competitive landscape and provides information on the products offered by various companies. To help clients improve their market positions, t his automated blood tube labeler and specimen transport box market forecast report provides a detailed analysis of the market leaders and offers information on the competencies and capacities of the companies. To make the most of the opportunities, market vendors should focus more on the growth prospects in the fast-growing segments, while maintaining their positions in the slow-growing segments. Although the benefits of automated labeling will offer immense business opportunities to the vendors, the high costs of devices will challenge the growth of many. are a few of the significant market participants. They are also offering products online to expand their geographic outreach. They are entering into agreements with GPOs and medical wholesalers to gain easy access to healthcare facilities and laboratories to increase sales. Key vendors are adopting innovative marketing strategies to increase their market penetration. The degree of fragmentation will remain the same over the forecast period. The automated blood tube labeler and specimen transport box market is currently fragmented. Request a FREE sample now! Market Competitive Analysis Market Overviewīrowse TOC and LoE with selected illustrations and example pages of automated blood tube labeler and specimen transport box market KG, Sonoco Products Co., Techno Medica Co. Also, the report analyzes the market’s competitive landscape and offers information on several market vendors, including Avantor Inc., Brooks Automation Inc., Cardinal Health Inc., Greiner AG, Inpeco SA, Kobayashi Create Co. This report provides a d etailed analysis of the market by product (automated blood tube labeler and specimen transport box) and geography (Asia, Europe, North America, and ROW). The market’s growth momentum will accelerate throughout the forecast period because of the steady increase in year-over-year growth. Our products comply with the IATA requirements for the transport of diagnostic specimens (UN packing instruction 602 and 650), assuming that our products are properly used (closed).The global automated blood tube labeler and specimen transport box market size has the potential to grow by USD 94.57 million during 2020-2024. Upon request, Micronic products can be supplied gamma irradiated or ethylene oxide treated. Micronic labware products are developed and manufactured in compliance with the European Directive 98/79/EC for In Vitro Diagnostic Medical Devices, Annex III. Products produced by Micronic are tested according to AQL inspection level G2 and AQL value 0.4. The 2D Data-Matrix code (which adheres to the ECC200 standard) and 1D barcode (type 128B) are laser-etched into the code area and are guaranteed unique. The Micronic 2D Data-Matrix codes and 1D barcodes are produced conform industry standards. Our products are periodically tested on RNase, DNase and their endotoxin levels by independent expert organizations. RNase, DNase and endotoxin (pyrogen)īy maintaining the highest possible hygiene level during our production processes, Micronic manufactured labware is free of any detectable RNase or DNase contamination and the endotoxin level of produced and packaged labware is limited to an acceptable minimum (< 0.01 EU/ml). One selection criteria is that no measurable amount of extractables should leach into samples. The materials used for Micronic tubes are the result of extensive research. Material components used to produce Micronic labware can be traced via the lot number indicated on the packaging. The materials are FDA approved and comply with the (USA) USP XXII tests, including class VI (Medical approved), and the European Pharmacopoeia-monograph 3.2.2 unless communicated otherwise. The raw materials and auxiliary agents are selected based on the specifications that satisfy the high quality requirements of our products. Virgin material and approvalsįor the manufacturing of its long term sample storage labware products Micronic uses solely virgin plastic raw material. Micronic labware is manufactured and assembled in-house in a NEN-EN-ISO14644-1 Class 7 certified clean room environment (which is comparable to the US Federal Standard 209E Class 10,000). The environmental policy of Micronic is determined by our headquarters in the Netherlands, which is certified to ISO 14001:2015. Reducing our impact on the environment is an integral part of our continuous improvement efforts. Micronic operates corporate integrated Quality Management System (QMS) that is certified to ISO 9001:2015. Our Standards Product Quality Information
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