Alcon 8065807001

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Cigna insurance find doctor	Accessories should be checked regularly. During initialization the drain pump is rotated to its home position. Connect the green male luer fitting to the stopcock see Figure Source Pressure parameter is Standard - When the source air pressure drops below a minimum level a popup window will acon stating that the operator must adjust supply source pressure to between 90 psi and psi. Position snap alcon 8065807001 along tubing to preferred location and snap closed.
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Alcon 8065807001	Never immerse in 88065807001 to cool. Upon Completion of Surgery Schedule: 1. Turn system power ON, and if required after initial self tests are completed, select Anterior mode of operation. Alternate irrigation pressure, set and enabled in the Irrigation Settings screen, is activated by pressing the footswitch's read article vertical switch. Please contact your local Alcon office for assistance in take-back options through Alcon or other providers.

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Contact Email. Email for the Customer contact; To be used by patients and consumers for device-related questions. Contact Phone. Phone number for the Customer contact; to be used by patients and consumers for device-related questions.

Contact Phone Extension. Size Type. Dimension type for the clinically relevant measurement of the medical device. Size Value. Numeric value for the clinically relevant size measurement of the medical device.

Size Unit of Measure. The unit of measure associated with each clinically relevant size. Size Text. Storage and Handling Type. Indicates storage and handling requirements that are required for the device including temperature, humidity, and atmospheric pressure. Storage and Handling High Value.

Indicates the high value for storage and handling requirements. Storage and Handling High Unit of Measure. Storage and Handling Low Value. Storage and Handling Low Unit of Measure. Storage and Handling Special Condition text. Device Packaged as Sterile. Indicates the medical device is free from viable microorganisms. Requires Sterilization Prior to Use. Sterilization Methods. Indicates the method s of sterilization that can be used for this device prior to device use on the patient.

Device Count. Device Exempt from Premarket Submission. Indicates that the product contains or consists of human cells or tissues that are intended for implantation, transplantation, infusion, or transfer into a human recipient as defined under 21 CFR Indicates that the device is a convenience, combination, in vitro diagnostic IVD , or medical procedure kit. Combination Product. Indicates that the product is comprised of two or more regulated products that are physically, chemically, or otherwise combined or mixed and produced as a single entity; packaged together as a single package; or packaged separately for the intended use together as defined under 21 CFR 3.

For Single-Use. Indicates that the device is intended for one use or on a single patient during a single procedure. Lot or Batch Number on Label. The number assigned to one or more device s that consist of a single type, model, class, size, composition, or software version that are manufactured under essentially the same conditions and that are intended to have uniform characteristics and quality within specified limits.

Serial Number on Label. The number that allows for the identification of a device, indicating its position within a series. Manufacturing Date on Label. The date on which a device is manufactured. Expiration Date on Label. The date by which the label of a device states the device must or should be used.

Donation Identification Number on Label. Indicates that the device or packaging contains natural rubber that contacts humans as described under 21 CFR Device labeled as "Not made with natural rubber latex". Indicates that natural rubber latex was not used as materials in the manufacture of the medical product and container and the device labeling contains this information.

Magnetic Resonance Imaging Safety Status. Prescription Use Rx. See 21 CFR The device may or may not still be available for purchase in the marketplace. Contact Phone WEB.

COM Phone number for the Customer contact; to be used by patients and consumers for device-related questions. Device Characteristics Device Count 1 Number of medical devices in the base package. Kits are a collection of products, including medical devices, that are packaged together to achieve a common intended use and is being distributed as a medical device. Combination Product FALSE Indicates that the product is comprised of two or more regulated products that are physically, chemically, or otherwise combined or mixed and produced as a single entity; packaged together as a single package; or packaged separately for the intended use together as defined under 21 CFR 3.

At least one of the products in the combination product must be a device in this case. Lot or Batch Number on Label TRUE The number assigned to one or more device s that consist of a single type, model, class, size, composition, or software version that are manufactured under essentially the same conditions and that are intended to have uniform characteristics and quality within specified limits. This number is required to be part of the UDI when included on the label in order to provide the means to track the device back to its manufacturing source or otherwise allow the history of the device manufacturing, packaging, labeleing, distribution and use to be determined.

This date is required to be part of the UDI when included on the label in order to provide the means to track the device back to its manufacturing source or otherwise allow the history of the device manufacturing, packaging, labeleing, distribution and use to be determined.

Device required to be labeled as containing natural rubber latex or dry natural rubber 21 CFR Device labeled as "Not made with natural rubber latex" TRUE Indicates that natural rubber latex was not used as materials in the manufacture of the medical product and container and the device labeling contains this information. Only applicable to devices not subject to the requirements under 21 CFR Not all medical products that are NOT made with natural rubber latex will be marked.

Similar Medical Devices. Company Name. Brand Name. Version or Model Number. The version or model found on the device label or accompanying packaging used to identify a category or design of a device. Catalog Number. The catalog, reference, or product number found on the device label or accompanying packaging to identify a particular product.

Device Description. Additional relevant information about the device that is not already captured as a distinct GUDID data attribute. Device Record Status. DI Record Publish Date. Commercial Distribution End Date.

Indicates the date the device is no longer held or offered for sale by the labeler on record. Commercial Distribution Status. Indicates whether the device is in commercial distribution as defined under 21 CFR Device Identifier Type.

Device Unique Identifier. Issuing Agency. Contains DI Number. Quantity Per Package. Package Discontinue Date. Indicates the date this particular package configuration is discontinued by the labeler. Package Status. Indicates whether the package is in commercial distribution as defined under 21 CFR FDA Product Code. Contact Email. Email for the Customer contact; To be used by patients and consumers for device-related questions.

Contact Phone. Phone number for the Customer contact; to be used by patients and consumers for device-related questions. Contact Phone Extension. Size Type. Dimension type for the clinically relevant measurement of the medical device.