Adult Renal Clamps – Left KS-2001

GUDID B033KS20010

Adult Renal Clamps – Left

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 IDB033KS20010
NIH Device Record Keya21e26d9-c99e-4e7b-983e-49e5e9ea3ed7
Commercial Distribution StatusIn Commercial Distribution
Brand NameAdult Renal Clamps – Left
Version Model NumberKS-2001
Catalog NumberKS-2001
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

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB033KS20010 [Primary]

FDA Product Code

DXCClamp, Vascular

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

Moist Heat or Steam Sterilization


[B033KS20010]

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

Devices Manufactured by Kapp Surgical Instrument Co.

B033KS400140 - Coned Heparin Needles2023-06-22 Coned Heparin Needles – Size 01 - 4in
B033KS400170 - Coned Heparin Needles2023-06-22 Coned Heparin Needles – Size 01 - 7in
B033KS400240 - Coned Heparin Needles2023-06-22 Coned Heparin Needles – Size 02 - 4in
B033KS400270 - Coned Heparin Needles2023-06-22 Coned Heparin Needles – Size 02 - 7in
B033KS400340 - Coned Heparin Needles2023-06-22 Coned Heparin Needles – Size 03 - 4in
B033KS400370 - Coned Heparin Needles2023-06-22 Coned Heparin Needles – Size 03 - 7in
B033KS400440 - Coned Heparin Needles2023-06-22 Coned Heparin Needles – Size 04 - 4in
B033KS400470 - Coned Heparin Needles2023-06-22 Coned Heparin Needles – Size 04 - 7in

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.