EXTRACTOR

GUDID 00888118128140

COMEDONE, KATSCH, W/PROTECTIVE METAL CAP

KLS-Martin L.P.

Bone curette, reusable

• Primary Device ID: 00888118128140
• NIH Device Record Key: a0912d51-0bff-481e-917f-8f4011b2655c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EXTRACTOR
• Version Model Number: 28-294-14-07
• 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

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	00888118128140 [Primary]

FDA Product Code

• FZS: CURETTE, SURGICAL, GENERAL USE

Sterilization

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

[00888118128140]

Moist Heat or Steam Sterilization

[00888118128140]

Moist Heat or Steam Sterilization

[00888118128140]

Moist Heat or Steam Sterilization

[00888118128140]

Moist Heat or Steam Sterilization

[00888118128140]

Moist Heat or Steam Sterilization

[00888118128140]

Moist Heat or Steam Sterilization

[00888118128140]

Moist Heat or Steam Sterilization

[00888118128140]

Moist Heat or Steam Sterilization

[00888118128140]

Moist Heat or Steam Sterilization

[00888118128140]

Moist Heat or Steam Sterilization

[00888118128140]

Moist Heat or Steam Sterilization

[00888118128140]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-08-26
• Device Publish Date: 2020-05-22

On-Brand Devices [EXTRACTOR]

• 00888118054784: 28-263-14-07
• 00888118054777: 28-261-14-07
• 00888118128140: COMEDONE, KATSCH, W/PROTECTIVE METAL CAP