FDA UDI In Commercial Distribution 🇺🇸 United States

GARRETT VASCULAR DILATOR

DI: 00192896010680 · Model: 2700-020 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
GARRETT VASCULAR DILATOR
Primary DI
00192896010680
Version / Model
2700-020
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-24
Public Version
1
Public Version Date
2018-09-24
Public Version Status
New
Public Device Record Key
e4d3ae2c-c3d0-42e5-ab17-77d08de2e611

Device Description

GARRETT VASCULAR DILATOR SET OF 3

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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
DWP Dilator, Vessel, Surgical

GMDN Terms

Code Name
11268 Vascular dilator, reusable

Identifiers

Type ID
Previous B09927000200
Primary 00192896010680

Customer Contacts

Phone
303-790-9411

Premarket Submissions

Submission Number Supplement Number
K100518 000

Device Sizes

Type Value Unit Text
Length 8.25 Inch