DILATOR

GUDID 00888118068989

KLS-Martin L.P.

Dental osteotome

• Primary Device ID: 00888118068989
• NIH Device Record Key: b5d42e34-bd83-4df7-9677-eefbfb2c9460
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DILATOR
• Version Model Number: 43-611-01-07
• Company DUNS: 826499238
• Company Name: KLS-Martin L.P.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888118068989 [Primary]

FDA Product Code

• EIX: PROBE, PERIODONTIC

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00888118068989]

Moist Heat or Steam Sterilization

[00888118068989]

Moist Heat or Steam Sterilization

[00888118068989]

Moist Heat or Steam Sterilization

[00888118068989]

Moist Heat or Steam Sterilization

[00888118068989]

Moist Heat or Steam Sterilization

[00888118068989]

Moist Heat or Steam Sterilization

[00888118068989]

Moist Heat or Steam Sterilization

[00888118068989]

Moist Heat or Steam Sterilization

[00888118068989]

Moist Heat or Steam Sterilization

[00888118068989]

Moist Heat or Steam Sterilization

[00888118068989]

Moist Heat or Steam Sterilization

[00888118068989]

Moist Heat or Steam Sterilization

[00888118068989]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-08-23
• Device Publish Date: 2018-09-26

On-Brand Devices [DILATOR]

• 10888118002034: 00-101-17-07
• 10888118002027: 00-101-16-07
• 00888118120984: 48-265-55-14
• 00888118055934: 35-180-03-07
• 00888118055927: 35-180-02-07
• 00888118055910: 35-180-01-07
• 00888118071453: 48-265-55-07
• 00888118068996: 43-611-02-07
• 00888118068989: 43-611-01-07
• 00888118068972: 43-610-02-07
• 00888118068965: 43-610-01-07
• 00888118055378: 32-460-14-01
• 00888118055361: 32-460-12-01
• 00888118055354: 32-430-26-01
• 00888118055347: 32-430-24-01
• 00888118055330: 32-430-22-01
• 00888118055323: 32-430-20-01
• 00888118055316: 32-430-18-01
• 00888118055309: 32-430-16-01
• 00888118055293: 32-430-14-01
• 00888118055286: 32-430-12-01
• 00888118055279: 32-430-10-01
• 00888118055262: 32-430-08-01
• 00888118055255: 32-430-06-01
• 00888118055248: 32-430-04-01
• 00888118055231: 32-430-02-01
• 00888118055217: 31-599-20-07
• 00888118055200: 31-599-18-07
• 00888118054586: 27-115-14-07
• 00888118054579: 27-113-14-07