RONGEUR

GUDID 00888118121721

KLS-Martin L.P.

Craniofacial rongeur, reusable Craniofacial rongeur, reusable Craniofacial rongeur, reusable Craniofacial rongeur, reusable Craniofacial rongeur, reusable Craniofacial rongeur, reusable Craniofacial rongeur, reusable Craniofacial rongeur, reusable Craniofacial rongeur, reusable Craniofacial rongeur, reusable Craniofacial rongeur, reusable Craniofacial rongeur, reusable Craniofacial rongeur, reusable Craniofacial rongeur, reusable Craniofacial rongeur, reusable Craniofacial rongeur, reusable
Primary Device ID00888118121721
NIH Device Record Key6804c207-6955-48b3-a2ef-5158dbf1ed33
Commercial Distribution StatusIn Commercial Distribution
Brand NameRONGEUR
Version Model Number37-364-03-07
Company DUNS826499238
Company NameKLS-Martin L.P.
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100888118121721 [Primary]

FDA Product Code

KBBRONGEUR, NASAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


[00888118121721]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-09-18
Device Publish Date2019-05-07

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0088811805925337-356-17-07
0088811805924637-343-12-07
0088811805923937-342-12-07
0088811805922237-341-13-07

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