Martinez Clamp KS-9999MCR

GUDID B033KS9999MCR0

Martinez Clamp – Right (7”)

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 IDB033KS9999MCR0
NIH Device Record Key414df230-cf87-40ba-8068-10ec81086459
Commercial Distribution StatusIn Commercial Distribution
Brand NameMartinez Clamp
Version Model NumberKS-9999MCR
Catalog NumberKS-9999MCR
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
HIBCCB033KS9999MCR0 [Primary]

FDA Product Code

DXCClamp, Vascular

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-21
Device Publish Date2023-06-13

On-Brand Devices [Martinez Clamp]

B033KS9999MCR0Martinez Clamp – Right (7”)
B033KS9999MCL0Martinez Clamp – Left (7”)
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