Contact: Steve Larsen - Sales Manager
Address: 1685 Marthaler Lane, West St. Paul, Minnesota 55118-3537, USA
Phone: +1-(651)-455-1611, 800-535-1998 | Fax: +1-(651)-450-8403 | Map/Directions >>

Profile: Tapemark is a specialty contract manufacturer focusing on the pharmaceutical, medical device, and consumer products industries. Our manufacturing facilities include multiple class 100,000 clean room suites where we offer integrated converting capabilities including coating/dispensing, laminating, die cutting, folding, printing, and packaging. We specialize in the custom converting of medical devices and components utilizing materials such as films, foils, foams, gels, nonwovens and hydrocolloids. We are an experienced contract manufacturer of custom components for in-vitro, non-invasive and molecular diagnostics and biosensor applications. Our expertise in both medical devices and pharmaceutical products provides a strong foundation in drug/device combination products. We also specialize in the addition of active ingredients to dressings and patches including antimicrobials, analgesics and other drug compounds.

The company was founded in 1952, has revenues of USD 50-100 Million, has ~200 employees and is ISO 9001, ISO 13485 certified.

FDA Registration Number: 2182681

21 Products/Services (Click for related suppliers)  
• Active Transdermal Patches
• Aromatherapy Patches
• Cannula Holder
• Catheter Guide Holder
• Contract Manufacturing
• Contract Packaging
• Device Label
• Disposable Product Contract Manufacturing
• Iontophoresis Device (FDA Code: KTB / 890.5525)
An iontophoresis device is a device that is intended to use a direct current to introduce ions of soluble salts or other drugs into the body and induce sweating for use in the diagnosis of cystic fibrosis or for other uses if the labeling of the drug intended for use with the device bears adequate directions for the device's use with that drug. When used in the diagnosis of cystic fibrosis, the sweat is collected and its composition and weight are determined.
• Nasal Dilator (FDA Code: LWF / 874.3900)
A nasal dilator is a device intended to provide temporary relief from transient causes of breathing difficulties resulting from structural abnormalities and/or transient causes of nasal congestion associated with reduced nasal airflow. The device decreases airway resistance and increases nasal airflow. The external nasal dilator is constructed from one or more layers of material upon which a spring material is attached, with a skin adhesive applied to adhere to the skin of the nose; it acts with a pulling action to open the nares. The internal nasal dilator is constructed from metal or plastic and is placed inside the nostrils; it acts by pushing the nostrils open or by gently pressing on the columella.
• Non-Invasive Sensors and Disposables
• Operating Room Assistance Devices
• Passive Transdermal Patches
• Pharmaceuticals/Chemicals Contract Manufacturing
• Pharmacy Labels
• Printers & Labels
• Probe Shields
• Reagent Contract Manufacturing
• Suture Strips
• Topical Patches
• Wound Dressings

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