DILATOR

GUDID 00888118120984

KLS-Martin L.P.

Dental osteotome
Primary Device ID00888118120984
NIH Device Record Keyce24a1b2-c1b8-4a3f-9010-e691a8856120
Commercial Distribution StatusIn Commercial Distribution
Brand NameDILATOR
Version Model Number48-265-55-14
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
GS100888118120984 [Primary]

FDA Product Code

LWFDILATOR, NASAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


[00888118120984]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-10-30
Device Publish Date2019-10-22

On-Brand Devices [DILATOR]

1088811800203400-101-17-07
1088811800202700-101-16-07
0088811812098448-265-55-14
0088811805593435-180-03-07
0088811805592735-180-02-07
0088811805591035-180-01-07
0088811807145348-265-55-07
0088811806899643-611-02-07
0088811806898943-611-01-07
0088811806897243-610-02-07
0088811806896543-610-01-07
0088811805537832-460-14-01
0088811805536132-460-12-01
0088811805535432-430-26-01
0088811805534732-430-24-01
0088811805533032-430-22-01
0088811805532332-430-20-01
0088811805531632-430-18-01
0088811805530932-430-16-01
0088811805529332-430-14-01
0088811805528632-430-12-01
0088811805527932-430-10-01
0088811805526232-430-08-01
0088811805525532-430-06-01
0088811805524832-430-04-01
0088811805523132-430-02-01
0088811805521731-599-20-07
0088811805520031-599-18-07
0088811805458627-115-14-07
0088811805457927-113-14-07

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