FDA UDI Not in Commercial Distribution 🇺🇸 United States

BAYONET SUCTION TUBE

DI: B0994129100 · Model: 412-910 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
BAYONET SUCTION TUBE
Primary DI
B0994129100
Version / Model
412-910
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
6
Public Version Date
2024-03-25
Public Version Status
Update
Public Device Record Key
c98d5027-d9ea-479b-8554-118a0ca8f8ae
Distribution End Date
2018-09-21

Device Description

BAYONET SUCTION TUBE RIGHT 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
Primary B0994129100

Customer Contacts

Device Sizes

Type Value Unit Text
Length 3.375 Inch
Device Size Text, specify 9 French Inner Diameter