FDA UDI In Commercial Distribution 🇺🇸 United States

COOLEY SUBRAMANIAN AORTIC CLAMP

DI: 00192896010086 · Model: 2100-143 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
COOLEY SUBRAMANIAN AORTIC CLAMP
Primary DI
00192896010086
Version / Model
2100-143
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
bf63b97a-3eb5-4b49-b68f-6b9ab6c19151

Device Description

COOLEY SUBRAMANIAN AORTIC CLAMP ANGLED JAW

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
No
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 B09921001430
Primary 00192896010086

Customer Contacts

Phone
8008217496

Premarket Submissions

Submission Number Supplement Number
K092544 000

Device Sizes

Type Value Unit Text
Length 6.25 Inch