FDA UDI Not in Commercial Distribution 🇺🇸 United States

FUKUSHIMA SUCTION TUBE

DI: B0991803900 · Model: 180-390 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FUKUSHIMA SUCTION TUBE
Primary DI
B0991803900
Version / Model
180-390
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
8
Public Version Date
2020-04-20
Public Version Status
Update
Public Device Record Key
6fae3b25-f4f6-42d3-8914-7b4cb00670c2
Distribution End Date
2018-06-18

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
Primary B0991803900

Customer Contacts

Phone
8008217496

Device Sizes

Type Value Unit Text
Length 6.5 Inch
Device Size Text, specify 10 French Inner Diameter