FDA UDI Not in Commercial Distribution 🇺🇸 United States

BAYONET SUCTION TUBE

DI: B0994129020 · Model: 412-902 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BAYONET SUCTION TUBE
Primary DI
B0994129020
Version / Model
412-902
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
5
Public Version Date
2018-09-21
Public Version Status
Update
Public Device Record Key
47885989-3f0a-4b62-be28-ae17be0b6913
Distribution End Date
2018-09-21

Device Description

BAYONET SUCTION TUBE TOP FINGER CONTROL

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
45254 Suction cannula, reusable

Identifiers

Type ID
Primary B0994129020

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 3.375 Inch
Device Size Text, specify 7 French Inner Diameter