FDA.reportPublic FDA data

Cardiopulmonary bypass cannula holder set

Primary DI
10803622106085
Brand
Cardiopulmonary bypass cannula holder set
Company
LIVANOVA USA, INC.
Model
TS-xxxxx
Published
2015-07-16
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
DWFCATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K000830000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K000830000CANNULATION TOURNIQUET SET, 2 TUBE OR 5 TUBECalifornia Medical Laboratories, Inc.2000-09-07DWF

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10803622106085PackageGS120In Commercial Distribution
00803622106088PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1080362210608510803622106085
00803622106088008036221060888036221060880803622106088

GMDN Terms#

Term, Definition table
TermDefinition
Cardiopulmonary bypass cannula holder setA collection of sterile devices intended to help secure a cardiopulmonary bypass cannula to the underlying tissue in the operative field to minimize displacement of the cannula during cardiopulmonary bypass surgery. Popularly known as a `snugger?, it typically consists of a number of colour-coded plastic tubes which can be cut to length, and a metal wire snare. The snare is intended to grasp a purse-string suture and to pull it taut through the tube; a holding suture is tied around the tube and the cannula to keep the cannula in place. This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
080914995
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

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