DeSoutter

GUDID 00810041638250

Provision

Laparoscopic access cannula, reprocessed

• Primary Device ID: 00810041638250
• NIH Device Record Key: 7a7d435e-d619-40de-9e4d-60f1808fede0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DeSoutter
• Version Model Number: S89-9656
• Company DUNS: 016889401
• Company Name: Provision
• Device Count: 1
• DM Exempt: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810041638250 [Primary]

FDA Product Code

• NBH: Accessories, Arthroscopic

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: 2020-05-21
• Device Publish Date: 2020-05-13

On-Brand Devices [DeSoutter]

• B504OMS8996560: S89-9656
• B504OMS8936560: S89-3656
• B504OMS8605340: S86-0534
• 00810041638250: S89-9656
• 00810041638243: S89-3656
• 00810041638236: S86-0534
• B504OMS8614350: S86-1435
• B504OMS8966560: S89-6656
• B504OMS8606320: S86-0632
• B504OMS8605120: S86-0512
• B504OMS1567560: S15-6756