FDA UDI Not in Commercial Distribution 🇺🇸 United States

FUKUSHIMA SUCTION TUBE

DI: B0991803810 · Model: 180-381 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FUKUSHIMA SUCTION TUBE
Primary DI
B0991803810
Version / Model
180-381
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
29a2e0eb-a1de-4a1b-8f72-e252392d8f99
Distribution End Date
2018-09-20

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
["Dry Heat Sterilization", "Moist Heat or Steam 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 B0991803810

Device Sizes

Type Value Unit Text
Length 8 Inch
Device Size Text, specify 11 French Inner Diameter