Single Pass Tunneling Guidewire - Small

Primary DI
00866614000146
Brand
Single Pass Tunneling Guidewire - Small
Company
ARKIS BIOSCIENCES INC.
Model
41.157.101
Catalog number
41.157.101
Device description
The Single Pass Tunneling Guidewire kit is designed to facilitate the subcutaneous passage of shunt tubing from a frontal scalp incision, or an incision on the neck, to an incision site on the torso when implanting a ventricular shunting system in patients greater than five (5) years old with a normal skull and normal skin.
Published
2018-12-14
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
MR Unsafe
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
GYKInstrument, Shunt System Implantation

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GYKInstrument, Shunt System ImplantationNeurology1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00866614000146PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00866614000146008666140001468666140001460866614000146

GMDN Terms#

Term, Definition table
TermDefinition
Subcutaneous tunneller, single-useA sterile, hand-held manual surgical instrument designed to create a subcutaneous tunnel (artificial passageway) between percutaneous entry and exit incisions for the subcutaneous placement of a device (e.g., catheter for medication administration, shunt). It is available in a variety of forms and may be: 1) a luminal sheath with a removable inner obturator, intended for co-axial device introduction, followed by sheath removal; or 2) a non-luminal device intended to either lead or pull the device through subcutaneous tissue. It is not intended for tunnelling through deep tissues. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
8442475383customerservice@arkisbiosciences.com
+1(800)654-2873custserv@integralife.com

Regulatory Flags#

DUNS number
078846878
Device count
1
Premarket exempt
true
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10866614000181Subcutaneous Guidewire - Medium41.240.50241.240.5022018-12-14
10866614000198Subcutaneous Guidewire - Large41.240.50341.240.5032018-12-14
10866614000105CerebroFlo EVD Catheter Set37.550.50137.550.5012019-10-24
00866614000115Galea Elevator41.312.10141.312.1012019-04-25
00866614000108CerebroFlo EVD Catheter Set37.550.10137.550.1012017-12-15
00866614000122Single Pass Tunneling Guidewire - Large41.157.10341.157.1032018-12-14
00866614000139Single Pass Tunneling Guidewire - Medium41.157.10241.157.1022018-12-14
00866614000153Precision Tunneler - Small41.020.50141.020.5012018-12-13
00866614000160Precision Tunneler - Medium41.020.50241.020.5022018-12-13
00866614000177Precision Tunneler - Large41.020.50341.020.5032018-12-13

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