FDA UDI In Commercial Distribution 🇺🇸 United States

BAYONET SUCTION TUBE

DI: 00192896001435 · Model: 412-900 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BAYONET SUCTION TUBE
Primary DI
00192896001435
Version / Model
412-900
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-21
Public Version
3
Public Version Date
2020-04-20
Public Version Status
Update
Public Device Record Key
7624f8d2-4556-4b69-a200-d973198500fd

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

Identifiers

Type ID
Previous B0994129000
Primary 00192896001435

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Device Size Text, specify 5 French Inner Diameter
Length 3.375 Inch