LCCS

GUDID 14895233607026

AN-SII SPINAL NEEDLE

LCCS Products Limited

Spinal needle, single-use

• Primary Device ID: 14895233607026
• NIH Device Record Key: 9d10f7dc-85ec-4dd8-a140-f00471810de8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LCCS
• Version Model Number: SS2790-LC
• Company DUNS: 663190222
• Company Name: LCCS Products Limited
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com
• Phone: +1 (844) 743-6449
• Email: info@lccsmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04895233607029 [Primary]
GS1	14895233607026 [Package]; Contains: 04895233607029; Package: Box [25 Units]; In Commercial Distribution
GS1	64895233607021 [Package]; Package: Carton [40 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131006

FDA Product Code

• BSP: Needle, Conduction, Anesthetic (W/Wo Introducer)

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-08-02
• Device Publish Date: 2021-07-24

On-Brand Devices [LCCS]

• 64895233608912: AN-E EPIDURAL NEEDLE
• 64895233608745: AN-E EPIDURAL NEEDLE
• 64895233608714: AN-E EPIDURAL NEEDLE
• 64895233608639: AN-E EPIDURAL NEEDLE
• 64895233608615: AN-E EPIDURAL NEEDLE
• 64895233608516: AN-E EPIDURAL NEEDLE
• 64895233608110: AN-E EPIDURAL NEEDLE
• 64895233608011: AN-E EPIDURAL NEEDLE
• 64895233606864: AN-SI SPINAL NEEDLE
• 64895233606710: AN-SI SPINAL NEEDLE
• 64895233606543: AN-SI SPINAL NEEDLE
• 64895233606536: AN-SI SPINAL NEEDLE
• 64895233606529: AN-SI SPINAL NEEDLE
• 64895233606437: AN-SI SPINAL NEEDLE
• 64895233606420: AN-SI SPINAL NEEDLE
• 64895233606246: AN-SI SPINAL NEEDLE
• 64895233606239: AN-SI SPINAL NEEDLE
• 64895233606222: AN-SI SPINAL NEEDLE
• 64895233605249: LCCS Radiofrequency (RF) Electrode
• 64895233605232: LCCS Radiofrequency (RF) Electrode
• 64895233605225: LCCS Radiofrequency (RF) Electrode
• 64895233605218: LCCS Radiofrequency (RF) Electrode
• 64895233605034: LCCS Radiofrequency (RF) Electrode
• 64895233605027: LCCS Radiofrequency (RF) Electrode
• 64895233605010: LCCS Radiofrequency (RF) Electrode
• 64895233602521: Single-use RF Cannula
• 64895233602422: Single-use RF Cannula
• 64895233602323: Single-use RF Cannula
• 64895233602316: Single-use RF Cannula
• 64895233602132: Single-use RF Cannula
• 64895233602026: Single-use RF Cannula
• 64895233601968: Single-use RF Cannula
• 64895233601913: Single-use RF Cannula
• 64895233601838: Single-use RF Cannula
• 64895233601746: Single-use RF Cannula
• 64895233601432: Single-use RF Cannula
• 64895233601326: Single-use RF Cannula
• 64895233601319: Single-use RF Cannula
• 64895233601142: Single-use RF Cannula
• 04895233601027: Single-use RF Cannula
• 14895233608832: AN-E EPIDURAL NEEDLE
• 14895233608825: AN-E EPIDURAL NEEDLE
• 14895233608818: AN-E EPIDURAL NEEDLE
• 14895233608733: AN-E EPIDURAL NEEDLE
• 14895233608726: AN-E EPIDURAL NEEDLE
• 14895233608627: AN-E EPIDURAL NEEDLE
• 14895233608429: AN-E EPIDURAL NEEDLE
• 14895233608412: AN-E EPIDURAL NEEDLE
• 14895233608337: AN-E EPIDURAL NEEDLE
• 14895233608320: AN-E EPIDURAL NEEDLE