SAW

GUDID 00888118030924

KLS-Martin L.P.

Manual surgical saw, rigid

• Primary Device ID: 00888118030924
• NIH Device Record Key: c2df87d0-c322-47f9-9a64-74397448f608
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SAW
• Version Model Number: 23-970-17-02
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888118030924 [Primary]

FDA Product Code

• GDR: SAW, MANUAL AND ACCESSORIES

Sterilization

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

[00888118030924]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-08-21
• Device Publish Date: 2018-09-26

On-Brand Devices [SAW]

• 00888118060235: 37-649-02-07
• 00888118060228: 37-649-01-07
• 00888118060211: 37-649-00-07
• 00888118060204: 37-633-20-07
• 00888118060198: 37-631-20-07
• 00888118030924: 23-970-17-02