INSUFLOW 6198M

GUDID 00852588007038

LAPAROSCOPIC GAS CONDITIONING DEVICE

LEXION MEDICAL, LLC

Insufflation gas conditioning tubing set

• Primary Device ID: 00852588007038
• NIH Device Record Key: f238a0d0-bc97-4493-b1cc-38f8393383a0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INSUFLOW
• Version Model Number: 6198M
• Catalog Number: 6198M
• Company DUNS: 848693730
• Company Name: LEXION MEDICAL, LLC
• 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: 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	00852588007038 [Primary]

FDA Product Code

• HIF: Insufflator, Laparoscopic

Sterilization

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

[00852588007038]

Ethylene Oxide

[00852588007038]

Ethylene Oxide

[00852588007038]

Ethylene Oxide

[00852588007038]

Ethylene Oxide

[00852588007038]

Ethylene Oxide

[00852588007038]

Ethylene Oxide

[00852588007038]

Ethylene Oxide

[00852588007038]

Ethylene Oxide

[00852588007038]

Ethylene Oxide

[00852588007038]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-02-15

On-Brand Devices [INSUFLOW]

• 00852588007038: LAPAROSCOPIC GAS CONDITIONING DEVICE
• 00852588007021: LAPAROSCOPIC GAS CONDITIONING DEVICE
• 00852588007014: Laparoscopic gas conditioning device
• 00852588007007: Laparoscopic gas conditioning device.