FDA UDI Not in Commercial Distribution 🇺🇸 United States

ABDOMINAL AORTIC CLAMP

DI: 00192896011205 · Model: 441-714 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ABDOMINAL AORTIC CLAMP
Primary DI
00192896011205
Version / Model
441-714
Catalog Number
441-714
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-15
Public Version
4
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
4391feb6-75b6-4380-a113-0fa12c84880f
Distribution End Date
2020-10-16

Device Description

ABDOMINAL AORTIC CLAMP ATRAUMATIC JAW CURVED SIDEWAYS

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
62470 Surgical bulldog clamp, reusable

Identifiers

Type ID
Primary 00192896011205

Customer Contacts

Phone
800-821-7496

Premarket Submissions

Submission Number Supplement Number
K092544 000

Device Sizes

Type Value Unit Text
Length 10 Inch