NIPPER

GUDID 00888118085696

KLS-Martin L.P.

Nail scissors, reusable

• Primary Device ID: 00888118085696
• NIH Device Record Key: 93202501-2390-4214-b9f2-baa08a781299
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NIPPER
• Version Model Number: 54-360-11-07
• 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
• 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 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	00888118085696 [Primary]

FDA Product Code

• FZT: CUTTER, SURGICAL

Sterilization

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

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

[00888118085696]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-08-23
• Device Publish Date: 2018-09-26

On-Brand Devices [NIPPER]

• 00888118103895: 54-336-14-07
• 00888118103499: 36-011-07-14
• 00888118103482: 36-011-06-14
• 00888118103475: 36-011-02-14
• 00888118103468: 36-011-01-14
• 00888118085696: 54-360-11-07
• 00888118070159: 47-572-11-07
• 00888118070142: 47-563-11-07
• 00888118056917: 36-011-01-02