Vasectomy Instruments K-9489

GUDID B033K94890

Vasectomy Forceps

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
Primary Device IDB033K94890
NIH Device Record Keyc7ea9ffd-4f17-4f30-b1f8-4d8c0fe603b7
Commercial Distribution StatusIn Commercial Distribution
Brand NameVasectomy Instruments
Version Model NumberK-9489
Catalog NumberK-9489
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 Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
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

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB033K94890 [Primary]

FDA Product Code

GDJClamp, Surgical, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B033K94890]

Moist Heat or Steam Sterilization


[B033K94890]

Moist Heat or Steam Sterilization


[B033K94890]

Moist Heat or Steam Sterilization


[B033K94890]

Moist Heat or Steam Sterilization


[B033K94890]

Moist Heat or Steam Sterilization


[B033K94890]

Moist Heat or Steam Sterilization


[B033K94890]

Moist Heat or Steam Sterilization


[B033K94890]

Moist Heat or Steam Sterilization


[B033K94890]

Moist Heat or Steam Sterilization


[B033K94890]

Moist Heat or Steam Sterilization


[B033K94890]

Moist Heat or Steam Sterilization


[B033K94890]

Moist Heat or Steam Sterilization


[B033K94890]

Moist Heat or Steam Sterilization


[B033K94890]

Moist Heat or Steam Sterilization


[B033K94890]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-19
Device Publish Date2023-06-09

On-Brand Devices [Vasectomy Instruments]

B033K95550Vasectomy Fixation Ring Clamp
B033K95540Vasectomy Forcep
B033K94900Fixation Ring Forcep
B033K94890Vasectomy Forceps

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