Today’s Trade Alerts include: Advanced ID Corp. (OTCBB: AIDO), Angiotech Pharmaceuticals Inc. (Nasdaq: ANPI), Level 3 Communications Inc. (Nasdaq: LVLT), Finisar Corp. (Nasdaq: FNSR), Beacon Power Corp. (Nasdaq: BCON) and Force Protection Inc. (Nasdaq: FRPT).
“Advanced ID Corp. (AIDO) shares jumped 20% to 24 cents in Wednesday’s mid-morning trading. Advanced ID is a complete solutions provider in the radio frequency identification (RFID) market. It utilizes low frequency (LF) radio waves for companion animal recovery purposes and ultra high frequency (UHF) waves for supply chain applications...
“The company recently announced it has received its first order from the Government of Taiwan for 5,000 LF RFID Pet Recovery Microchips. This initial order for Advanced ID Animal RFID products in Taiwan forms part of a yearly commitment of 100,000 chips per year as well as 1,000 readers per year…
“Advanced ID also announced its participation in a pig tagging/traceability project in Taiwan using the company’s UHF RFID Pig Ear Tag. This device is recognized for its unique design for long life and long read range. Its market potential is eight million tags per year according to the Taiwan agriculture department. In addition, the Taiwan government has been asked to assist the Fujian province in China in implementing a similar trace back system...”
“Angiotech Pharmaceuticals Inc. (ANPI) shares dropped 4.76% Wednesday morning, trading at $1.80. Angiotech is a global specialty pharmaceutical and medical device company that discovers, develops and markets innovative technologies and medical products primarily for local diseases or for complications associated with medical device implants, surgical interventions and acute injury…
“The company recently announced it has received CE Mark approval to begin marketing the HemoStream Chronic Dialysis Catheter in Europe. CE or Conformité Européenne (European Conformity) Mark is a mandatory European marking for certain product groups to indicate conformity with the essential health and safety requirements set out in European Directives…
“This CE Mark approval follows Angiotech's announcement in August 2007 that it had received clearance from the U.S. Food and Drug Association (FDA) to begin marketing HemoStream in the United States. In April last year, Angiotech entered into an agreement with Rex Medical, LP that granted Angiotech an exclusive license to market and distribute HemoStream worldwide…”
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