FDA UDI In Commercial Distribution 🇺🇸 United States

FUKUSHIMA SUCTION TUBE

DI: 00192896009684 · Model: 180-375 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
FUKUSHIMA SUCTION TUBE
Primary DI
00192896009684
Version / Model
180-375
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-20
Public Version
3
Public Version Date
2020-04-20
Public Version Status
Update
Public Device Record Key
798041df-18c5-457e-b714-bfb91a2b0b52

Device Description

FUKUSHIMA SUCTION TUBE

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

Product Codes

Code Name
JOL Catheter And Tip, Suction

GMDN Terms

Code Name
38749 Surgical/emergency suction cannula, non-illuminating, reusable

Identifiers

Type ID
Previous B0991803750
Primary 00192896009684

Customer Contacts

Phone
8008217496

Device Sizes

Type Value Unit Text
Device Size Text, specify 5 French Inner Diameter
Length 8 Inch