FDA UDI In Commercial Distribution 🇺🇸 United States

Precision Tunneler - Large

DI: 00866614000177 · Model: 41.020.503 · ARKIS BIOSCIENCES INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Precision Tunneler - Large
Primary DI
00866614000177
Version / Model
41.020.503
Catalog Number
41.020.503
Company Name
ARKIS BIOSCIENCES INC.
Labeler DUNS
078846878
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-13
Public Version
5
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
99cede43-4c8f-4802-a4e2-5cd3ac670539

Device Description

The Arkis Precision Tunneler is designed to facilitate the subcutaneous passage of shunt tubing between two skin incisions when implanting a ventricular shunting system in patients with normal skin.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GYK Instrument, Shunt System Implantation

GMDN Terms

Code Name
46801 Subcutaneous tunneller, single-use

Identifiers

Type ID
Primary 00866614000177

Customer Contacts