FDA UDI Not in Commercial Distribution 🇺🇸 United States

TUNNELER

DI: B09927001000 · Model: 2700-100 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TUNNELER
Primary DI
B09927001000
Version / Model
2700-100
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-19
Public Version
7
Public Version Date
2018-09-24
Public Version Status
Update
Public Device Record Key
0a522484-1c7c-4f2c-a2d4-acf5004c410b
Distribution End Date
2018-09-24

Device Description

TUNNELER

Device Characteristics

Single Use
No
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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
DWP Dilator, Vessel, Surgical

GMDN Terms

Code Name
35950 Vascular graft tunneller

Identifiers

Type ID
Primary B09927001000

Customer Contacts

Phone
303-790-9411

Premarket Submissions

Submission Number Supplement Number
K100518 000

Device Sizes

Type Value Unit Text
Length 20 Inch
Device Size Text, specify 1.5 Inch Handle