Baby Renal Clamp – Right KS-1002

GUDID B033KS10020

Baby Renal Clamp – Right

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 IDB033KS10020
NIH Device Record Key8b783037-6753-4d7a-9e21-cd9d23256920
Commercial Distribution StatusIn Commercial Distribution
Brand NameBaby Renal Clamp – Right
Version Model NumberKS-1002
Catalog NumberKS-1002
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com
Phone(216) 587-4400
Emailinfo@kappsurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB033KS10020 [Primary]

FDA Product Code

DXCClamp, Vascular

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

[B033KS10020]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-15
Device Publish Date2023-06-07

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