FDA UDI In Commercial Distribution 🇺🇸 United States

SUCTION TUBE

DI: 00192896101050 · Model: 412-739-2.5 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SUCTION TUBE
Primary DI
00192896101050
Version / Model
412-739-2.5
Catalog Number
412-739-2.5
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-23
Public Version
2
Public Version Date
2023-06-14
Public Version Status
Update
Public Device Record Key
d2d43c69-77d5-48b7-b7ff-254e6284d73a

Device Description

MICRO SUCTION IRRIGATION/ASPIRATION TUBE ANGLED

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
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
JOL CATHETER AND TIP, SUCTION

GMDN Terms

Code Name
64119 Surgical irrigation/aspiration cannula, non-illuminating, reusable

Identifiers

Type ID
Primary 00192896101050

Customer Contacts

Device Sizes

Type Value Unit Text
Length 4 Inch
Outer Diameter 2.5 Millimeter