Insufflator 50L

GUDID 04056702008895

W.O.M. World of Medicine GmbH

Laparoscopic insufflator Laparoscopic insufflator Laparoscopic insufflator Laparoscopic insufflator Laparoscopic insufflator Laparoscopic insufflator Laparoscopic insufflator Laparoscopic insufflator

• Primary Device ID: 04056702008895
• NIH Device Record Key: 073277b3-292d-43f6-a12a-132dbc27b923
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Insufflator 50L
• Version Model Number: ZEOSINSUFF
• Company DUNS: 316305242
• Company Name: W.O.M. World of Medicine GmbH
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04056702008895 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153513

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: 2020-11-09
• Device Publish Date: 2020-11-01

On-Brand Devices [Insufflator 50L]

• 04056702005771: FM134
• 04056702003227: FM134
• 04056702007218: FM134
• 04056702008895: ZEOSINSUFF