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Product Details:

Contraindication: This device used for any other purposes than for the indicated use is the responsibility of the user.

Indication:The ACT Plus® instrument is intended for in vitro diagnostic testing in either a hospital laboratory setting or a point of care (decentralized) setting (e.g., in the operating room, cardiac catheterization lab, intensive care unit, or clinic, etc.).

Warnings: Proper instrument and cartridge use. The instrument and cartridges must only be used in the manner and purpose for which they are intended. Instructions for proper use are included in the manual and in the cartridge insert package inserts. Read all warnings, precautions, and Instructions For Use carefully prior to use.

Caution: Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions For Use which accompany each product.

Additional Information:

• Production Capacity: act plus
• Delivery Time: 2-3
• Packaging Details: box packing

Product Details:

Sorin group (b)(4) received a report of poor oxygenation from the d901 lilliput oxygenator during a procedure. The clinician increased the oxygen level and the SORIN GROUP ITALIA D901 LILLIPUT 1 NEW BORN HOLLOW FIBER ... The oxygenator was changed out and the case proceeded without further issues
The D 901 LILLIPUT 1 OPEN SYSTEM is a NEW BORN oxygenator intended for use in ... SORIN GROUP ITALIA is not responsible for problems arising from
The D901 DIDECO LILLIPUT is a NEW BORN oxygenator intended for use in ... ENGLISH symbol non sterile on the pack) contact SORIN GROUP ITALIA 

Additional Information:

• Production Capacity: LONG TERM
• Delivery Time: 4-5 WORKING DAYS
• Packaging Details: 1BOX

Product Details:

INTRODUCER SHEATH (MEDTRONIC). HOW THE INPUT INTRODUCER SHEATH WORKS. Coronary catheterization is a minimally invasive procedure
 Medtronic Input TS Femoral Introducer Sheath with Needle and Guidewire for Angiographic Procedures 

Additional Information:

• Production Capacity: LONG TERM
• Delivery Time: 3-4 WORKING DAYS
• Packaging Details: 5PCS IN (1-BOX)

Product Details:

1952 | Ethicon1952-DE | Ethicon EMEASURGICEL Family of Absorbable Hemostats |EthiconEthicon Surgicel Powder Hemostat an alternative to Arista Powder. 1952, 1952, Loose knit of oxidized regenerated cellulose (ORC). Remove any excess before surgical closure in order to facilitate absorption and minimize the possibility of ..

Ethicon 1952 Surgicel Absorbable Hemostat, 4" x 8", 24/Cs ETHICON: 1952 - ETHICON SURGICEL HEMOSTAT ETHICON: 1952. ETHICON SURGICEL HEMOSTAT: ORIGINAL ABSORBABLE HEMOSTATSurgicel Absorbable Hemostat by Ethicon. Click to enlarge.  Manufacturer: Ethicon. The first and  ETH1952H, Sterile Surgicel. ETH1952Z, Sterile Surgicel

Additional Information:

• Packaging Details: 1BOX

Product Details:

Valleylab REM Polyhesive Adult Patient Return Electrode E7507

• For patients > 30 lbs (> 13.6 kg)
• Cord Length: 9' (2.7 m)
• For use with RECQM generators
• Latex free
• 50 Return electrodes per case
• Sold by the case
• Manufacturer: Covidien/Valleylab
• Manufacturer's ID: E7507

Covidien patient return electrodes are recognized worldwide for quality, safety, and innovative technology. All return electrodes are manufactured with Covidien's patented PolyHesive II high moisture, conductive adhesive hydrogel that provides the performance of a gel without the gel mess.

PolyHesive II Hydrogel Benefits

• Water-based hydrogel lowers skin resistance.
• Unique elongation fills patient skin irregularities and minimizes contact voids to improve the total electrical conduction area.

Electrode Benefits

• Surface area disperses current over large area, minimizing heat buildup.
• Acrylic adhesive improves pad contact quality and provides a moisture barrier to significantly reduce the potential for fluid invasion.
• Adult, infant (<30 lb.), and neonatal (<6 lb.) sizes available.
• Non-irritating* and non-sensitizing*

REM Contact Quality Monitoring System

• The exclusive Covidien REM™ system monitors patient impedance levels, automatically deactivating the generator if a fault at the patient return electrode is detected.
• REM™ is an integral part of the Covidien Full Circuit™ system standardization program.
• Proven safe in more than 100 million procedures.

*Testing done in accordance with FDA recommended ISO skin irritation study and ISO sensitization study.

Additional Information:

• Item Code: E7507
• Production Capacity: 50 Return electrodes per case Sold by the case
• Delivery Time: 2-3 WORKING DAYS
• Packaging Details: BOX PACKAGING