OASIS

GUDID 20650862110092

DRAIN, SINGLE, W/AC, TYVEK

ATRIUM MEDICAL CORPORATION

Thoracic suction system

• Primary Device ID: 20650862110092
• NIH Device Record Key: 942aec44-fd54-4d3d-b06a-1d73f82e8e74
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OASIS
• Version Model Number: 3600-130
• Company DUNS: 051798999
• Company Name: ATRIUM MEDICAL CORPORATION
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00650862110098 [Primary]
GS1	20650862110092 [Package]; Contains: 00650862110098; Package: [6 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K043140

FDA Product Code

• KDQ: Bottle, Collection, Vacuum

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-09-24

On-Brand Devices [OASIS]

• 20650862114014: DRAIN, DRY DUAL TOTAL REC W/AC
• 20650862113017: OASIS DRAIN, BRU, IN-LINE, ATS COMPATIBLE
• 20650862112010: OASIS DRAIN, DUAL, IN-LINE, ATS COMPATIBLE
• 20650862111020: DRAIN, DRY PEDIATRIC
• 20650862111013: OASIS DRAIN, PEDIATRIC INLINE & CLAMP
• 20650862110092: DRAIN, SINGLE, W/AC, TYVEK
• 20650862110054: DRAIN, DRY SINGLE - SFP
• 20650862110030: DRAIN, DRY SINGLE W/AC, ATS
• 20650862110016: OASIS DRAIN, SINGLE, INLINE & ATS COMPATIBLE