CALIPER

GUDID 00888118055897

KLS-Martin L.P.

General-purpose calliper, metallic

• Primary Device ID: 00888118055897
• NIH Device Record Key: 57c3f097-24e3-4f87-8e16-be1ffc6ceafb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CALIPER
• Version Model Number: 35-134-18-07
• 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	00888118055897 [Primary]

FDA Product Code

• FTY: TAPE, MEASURING, RULERS AND CALIPERS

Sterilization

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

[00888118055897]

Moist Heat or Steam Sterilization

[00888118055897]

Moist Heat or Steam Sterilization

[00888118055897]

Moist Heat or Steam Sterilization

[00888118055897]

Moist Heat or Steam Sterilization

[00888118055897]

Moist Heat or Steam Sterilization

[00888118055897]

Moist Heat or Steam Sterilization

[00888118055897]

Moist Heat or Steam Sterilization

[00888118055897]

Moist Heat or Steam Sterilization

[00888118055897]

Moist Heat or Steam Sterilization

[00888118055897]

Moist Heat or Steam Sterilization

[00888118055897]

Moist Heat or Steam Sterilization

[00888118055897]

Moist Heat or Steam Sterilization

[00888118055897]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-08-22
• Device Publish Date: 2018-09-26

On-Brand Devices [CALIPER]

• 00888118122476: 38-684-42-07
• 00888118117137: 99-535-90-01
• 00888118097347: 99-568-21-01
• 00888118072498: 48-420-00-07
• 00888118072306: 48-370-30-07
• 00888118072290: 48-370-26-07
• 00888118055903: 35-135-18-07
• 00888118055897: 35-134-18-07
• 00888118055880: 35-134-09-07
• 00888118055873: 35-133-09-07
• 00888118055866: 35-133-07-07
• 00888118055859: 35-133-06-07
• 00888118023094: 17-416-01-07
• 00888118023087: 17-407-01-07
• 00888118023070: 17-406-00-07
• 00888118008626: 04-407-20-07
• 00888118145888: UNIVERSAL, 0-150 MM