SAW

GUDID 00888118060235

KLS-Martin L.P.

Manual surgical saw, flexible

• Primary Device ID: 00888118060235
• NIH Device Record Key: ba1f570b-f8e2-4761-85c0-73f52d8283c6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SAW
• Version Model Number: 37-649-02-07
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888118060235 [Primary]

FDA Product Code

• KBC: SAW, NASAL

Sterilization

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

[00888118060235]

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 [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