Proxis™ Ureteral Access Sheath

Primary DI
00801741101687
Brand
Proxis™ Ureteral Access Sheath
Company
C. R. Bard, Inc.
Model
231035
Catalog number
231035
Device description
Proxis™ Ureteral Access Sheath
Published
2016-07-26
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
FEDendoscopic access overtube, gastroenterology-urology

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FEDEndoscopic Access Overtube, Gastroenterology-UrologyGastroenterology, Urology2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00801741101687PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00801741101687008017411016878017411016870801741101687

GMDN Terms#

Term, Definition table
TermDefinition
Ureteral dilatation/injection catheterA sterile, flexible or semi-flexible tube designed to be inserted through the urethra to open or increase the diameter of a constricted or irregular ureteral passage and allow the injection of a contrast medium to access possible submucosal tunnelling. The device is typically made of plastic materials and is available in a variety of diameters and lengths. It may also be used for the injection of a topical anaesthetic; other instruments may be passed through this device. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Catheter Gauge12French
Length35Centimeter

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)526-4455medical.services@crbard.com

Regulatory Flags#

DUNS number
016898496
Device count
1
Lot or batch
true
Expiration date on label
true

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