FDA UDI In Commercial Distribution 🇺🇸 United States

GARRETT VASCULAR DILATOR

DI: 00192896010703 · Model: 2700-050 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
GARRETT VASCULAR DILATOR
Primary DI
00192896010703
Version / Model
2700-050
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-29
Public Version
1
Public Version Date
2018-10-01
Public Version Status
New
Public Device Record Key
de730a86-7cdf-4e0b-89b9-b41d7af256c9

Device Description

GARRETT VASCULAR DILATOR SOFT MALLEABLE 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 B09927000500
Primary 00192896010703

Customer Contacts

Phone
303-790-9411

Premarket Submissions

Submission Number Supplement Number
K100518 000

Device Sizes

Type Value Unit Text
Length 5.5 Inch