FDA UDI In Commercial Distribution 🇺🇸 United States

BUIE RECTAL SUCTION TUBE

DI: 00192896001541 · Model: 508-523 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BUIE RECTAL SUCTION TUBE
Primary DI
00192896001541
Version / Model
508-523
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-22
Public Version
3
Public Version Date
2020-04-20
Public Version Status
Update
Public Device Record Key
de5c88bf-3cbe-404e-846a-7b332c99936c

Device Description

BUIE RECTAL SUCTION TUBE WITH FINGER VALVE

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Previous B0995085230
Primary 00192896001541

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Device Size Text, specify 15 French Inner Diameter
Length 16 Inch