BLADE

GUDID 00888118022523

KLS-Martin L.P.

Surgical retractor/retraction system blade, reusable

• Primary Device ID: 00888118022523
• NIH Device Record Key: ef66ca9e-647f-4820-9fc0-d5ffc2b9e845
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BLADE
• Version Model Number: 15-859-01-07
• 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	00888118022523 [Primary]

FDA Product Code

• GAD: RETRACTOR

Sterilization

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

[00888118022523]

Moist Heat or Steam Sterilization

[00888118022523]

Moist Heat or Steam Sterilization

[00888118022523]

Moist Heat or Steam Sterilization

[00888118022523]

Moist Heat or Steam Sterilization

[00888118022523]

Moist Heat or Steam Sterilization

[00888118022523]

Moist Heat or Steam Sterilization

[00888118022523]

Moist Heat or Steam Sterilization

[00888118022523]

Moist Heat or Steam Sterilization

[00888118022523]

Moist Heat or Steam Sterilization

[00888118022523]

Moist Heat or Steam Sterilization

[00888118022523]

Moist Heat or Steam Sterilization

[00888118022523]

Moist Heat or Steam Sterilization

[00888118022523]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-03-09
• Device Publish Date: 2018-09-26

On-Brand Devices [BLADE]

• 00888118114389: 38-709-07-07
• 00888118114372: 38-709-06-07
• 00888118022523: 15-859-01-07
• 00888118121875: 38-227-06-07
• 00888118121868: 38-227-05-07
• 00888118121844: 38-227-04-07
• 00888118121837: 38-227-03-07
• 00888118121820: 38-227-02-07
• 00888118118752: 995-5365-01
• 00888118107398: 15-859-02-07
• 00888118126054: 99-572-42-02
• 00888118063267: 38-708-03-07
• 00888118061867: 38-224-03-07
• 00888118061850: 38-224-02-07
• 00888118061843: 38-224-01-07
• 00888118061768: 38-212-05-07
• 00888118061751: 38-212-04-07
• 00888118061744: 38-212-03-07
• 00888118061737: 38-212-02-07
• 00888118061720: 38-212-01-07
• 00888118022370: 15-792-01-01
• 00888118003591: 01-004-83-07
• 00888118003584: 01-004-82-07
• 00888118003577: 01-004-81-07
• 00888118119445: 99-584-24-01
• 00888118116239: 99-584-24-02
• 00888118145994: PERIOTOME, NO. 2B, ANGLED, WIDE, FOR 23-360-01-07
• 00888118145987: PERIOTOME, NO. 1B, ANGLED, NARROW, FOR 23-360-01-07
• 00888118145970: PERIOTOME, NO. 2A, CURVED, WIDE, FOR 23-360-01-07
• 00888118145963: PERIOTOME, NO. 1A, CURVED, NARROW, FOR 23-360-01-07
• 00888118145956: PERIOTOME, NO. 2, STRAIGHT, WIDE, FOR 23-360-01-07
• 00888118145949: PERIOTOME, NO. 1, STRAIGHT, NARROW, FOR 23-360-01-07