Loop Aorta Clamp KS-7700

GUDID B033KS77000

Loop Aorta Clamp

Kapp Surgical Instrument Co.

Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable
Primary Device IDB033KS77000
NIH Device Record Key27d74ae9-e8fe-46a2-849f-2d2abf0954ed
Commercial Distribution StatusIn Commercial Distribution
Brand NameLoop Aorta Clamp
Version Model NumberKS-7700
Catalog NumberKS-7700
Company DUNS004171112
Company NameKapp Surgical Instrument Co.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com
Phone216-587-4400
Emailinfo@kappsurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB033KS77000 [Primary]

FDA Product Code

DXCClamp, Vascular

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-22
Device Publish Date2023-06-14

On-Brand Devices [Loop Aorta Clamp]

B033KS7700XL0Loop Aorta Clamp – Extra Long
B033KS77000Loop Aorta Clamp
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