Smith & Nephew Insufflator 500 72-00259-0

GUDID 00817183020677

Insufflator, Laparoscopic, 50LPM

NORTHGATE TECHNOLOGIES INC.

Laparoscopic insufflator

• Primary Device ID: 00817183020677
• NIH Device Record Key: 5ed48f0a-fc36-4629-9fdf-6039a342ed13
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Smith & Nephew Insufflator 500
• Version Model Number: 72203994
• Catalog Number: 72-00259-0
• Company DUNS: 627969264
• Company Name: NORTHGATE TECHNOLOGIES INC.
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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	00817183020677 [Primary]
GS1	03596010673497 [Previous]

FDA Product Code

• HIF: Insufflator, Laparoscopic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-08-14
• Device Publish Date: 2020-08-06

On-Brand Devices [Smith & Nephew Insufflator 500]

• 00817183020677: Insufflator, Laparoscopic, 50LPM
• 00817183020745: Insufflator, Laparoscopic, S&N 500 Service Replacement, 50LPM