Epson workforce pro wf-3720 user guide. At the core of this proprietary technology is the PrecisionCore MicroTFP print chip, a digital chip that produces dots at the micron level — 1/100th the size of a human hair. PRECISIONCORE INKJET TECHNOLOGYA truly innovative system, PrecisionCore features Epson's advanced thin-film piezoelectric (TFP ®) elements, which are produced via a MEMS manufacturing process, using semiconductor micro-fabrication techniques.
On October 18, 2013 the firm sent the following notification to their customers: This is to inform you of a product recall involving: Pinook s Mini-massager and Pinook s Micro Massager model number PT-11 See enclosed product label (for ease in identifying the product at retail/user level).
Jan 11, 2012 January 11, 2012. Us pinook mini massager – Pinook Portable Digital Personal Handheld Pocket Size Travel Mini Massager / Masseuse Dual Voltage 110v-240v Massage +2 Extra Pair of Pads. Regular movement of relevant muscle groups of the human body will bring out about the therapeutic effect of an actual manual massage. Jun 01, 2012 Pinook Medi Pro Mouse Massager Handheld Portable – 3 Modes + 2 Pairs of Pads + Free Extra Pair of Pads – Pinook USA. Regular movement of relevant muscle groups of the human body will bring out about the therapeutic effect of an actual manual massage. Use: The apparatus is for pain relief (sore muscles, joint. Zyllion Arc Handheld Mini.
Mar 20, 2014 Pinook Electric Massagers Pinook Electric Massagers in Mini, Micro Elite, or Nano2 Style. Hi what are the differences between those three massagers you offer pinook micro, mini and nano2 massager? Travel adaptor, user manual, and warranty card. From Groupon replied on Mar 20, 2014 1 - 4 of 4 questions. Buy products related to pinook mini massager products and see what customers say about pinook mini massager products on Amazon.com FREE DELIVERY possible on eligible purchases.
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| On October 18, 2013 the firm sent the following notification to their customers: This is to inform you of a product recall involving: Pinook0019s Mini-massager and Pinook0019s Micro Massager model number PT-11 See enclosed product label (for ease in identifying the product at retail/user level). This recall has been initiated due to failure to submit a premarket submission and gain approval. We began shipping this product on 11/27/2012. Immediately examine your inventory and quarantine product subject to recall. In addition, if you may have further distributed this product, please identify your customers and notify them at once of this product recall. Your notification to your customers may be enhanced by including a copy of this recall notification letter. Pinook USA is removing the products (mini and micro massager) from the market until receiving FDA approval to market them again under a new 510(k). If you have stock on your end please return them to our office: 901 C FL PKWY STE A6, Orlando FL, 32824. Before returning, please contact Sheva Ben-Shushan: accounting@pinookusa.com in order to receive an RMA number. Once you have RMA number, place that number on the package label. This recall should be carried out to the retail level. Your assistance is appreciated and necessary to prevent patient harm. If you have any questions, call Dvir Lev-Ran, telephone number: 407-854-0055 Ext 304. This recall is being made with the knowledge of the Food and Drug Administration. | |||||||||||||||||||||||||||
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| 28,994 units (Mini and Micro) | |||||||||||||||||||||||||||
| Worldwide Distribution-USA (nationwide) including Puerto Rico and Guam and the states of AZ, CA, CO, FL, IL, MA, MD, MO, MT, NC, ND, NJ, NV, NY, TX, VA, and WA and the country of Canada. | |||||||||||||||||||||||||||
| TPLC Device Report | |||||||||||||||||||||||||||
| 1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55. | |||||||||||||||||||||||||||