LaproClose LCLOSE-200

GUDID 00850067560180

LAPROCLOSE SUTURE PASSER, 150 MM SUTURE PASSOR, 14G, WITH TWO GUIDES (10/12 MM & 15 MM) AND TWO TROCAR EACH

Surgical Principals, Inc

Suturing unit, reusable

• Primary Device ID: 00850067560180
• NIH Device Record Key: d58d046f-3091-43cf-bc52-35b132b50e0c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LaproClose
• Version Model Number: LCLOSE-200
• Catalog Number: LCLOSE-200
• Company DUNS: 782873892
• Company Name: Surgical Principals, Inc
• Device Count: 10
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850067560180 [Unit of Use]
GS1	10850067560187 [Primary]

FDA Product Code

• HWQ: Passer

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: 2025-12-19
• Device Publish Date: 2025-12-11

On-Brand Devices [LaproClose]

• 00850067560197: LAPROCLOSE SUTURE PASSER, 180 MM SUTRURE PASSER, 14G, TWO BARIATRIC (XL) LENGTH GUIDES (10/12 MM
• 00850067560180: LAPROCLOSE SUTURE PASSER, 150 MM SUTURE PASSOR, 14G, WITH TWO GUIDES (10/12 MM & 15 MM) AND TWO
• 00850067560173: LAPROCLOSE SUTURE PASSER , 150 MM SUTURE PASSOR, 14G, WITH ONE GUIDE (10/12 MM) AND TWO TROCAR S