Lacrimal lntubation Set

GUDID 00845819000359

Lacrimal lntubation Set

OASIS MEDICAL, INC.

Lacrimal intubation set

• Primary Device ID: 00845819000359
• NIH Device Record Key: 7f4e0a70-90a5-4b66-9263-21c4f7f18997
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lacrimal lntubation Set
• Version Model Number: 6001
• Company DUNS: 194121018
• Company Name: OASIS MEDICAL, INC.
• Device Count: 1
• 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: false
• 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

Customer Support Contacts

• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com
• Phone: 9093055400
• Email: customerservice@oasismedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00845819000359 [Primary]
GS1	10845819000356 [Package]; Package: Plastic Bag [3 Units]; In Commercial Distribution

FDA Product Code

• OKS: Lacrimal Stents And Intubation Sets

Sterilization

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

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

[00845819000359]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-07-10
• Device Publish Date: 2023-06-30

On-Brand Devices [Lacrimal lntubation Set]

• 10845819000431: Lacrimal lntubation Set, 27g
• 00845819000397: DCR Set, Curved
• 00845819000380: DCR Set, Straight
• 00845819000359: Lacrimal lntubation Set
• 10845819000318: Lacrimal Intubation Set with Retrieval Device