FDA UDI In Commercial Distribution 🇺🇸 United States

DEBAKEY BAHNSON AORTIC CLAMP

DI: 00192896010444 · Model: 2100-6892 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DEBAKEY BAHNSON AORTIC CLAMP
Primary DI
00192896010444
Version / Model
2100-6892
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
2019-08-21
Public Version Status
Update
Public Device Record Key
ad734235-a567-419c-befa-95c443e036f6

Device Description

DEBAKEY BAHNSON AORTIC CLAMP "S" CURVED

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
No
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
DXC Clamp, Vascular

GMDN Terms

Code Name
62468 Surgical soft-tissue manipulation forceps, scissors-like, reusable

Identifiers

Type ID
Previous B099210068920
Primary 00192896010444

Customer Contacts

Phone
800-821-7496

Premarket Submissions

Submission Number Supplement Number
K092544 000

Device Sizes

Type Value Unit Text
Length 10.25 Inch