FDA UDI In Commercial Distribution 🇺🇸 United States

COUPLAND SUCTION TUBE

DI: 00192896009844 · Model: 412-676 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
COUPLAND SUCTION TUBE
Primary DI
00192896009844
Version / Model
412-676
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-24
Public Version
3
Public Version Date
2020-04-20
Public Version Status
Update
Public Device Record Key
a66857e1-8b94-43bc-9f57-20780fedbf7d

Device Description

COUPLAND SUCTION TUBE #4

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 B0994126760
Primary 00192896009844

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 6.5 Inch
Device Size Text, specify 3.5mm Tip