EXPRESS

GUDID 20650862199301

EXPRESS MINI 500 SUCTION BULB

ATRIUM MEDICAL CORPORATION

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• Primary Device ID: 20650862199301
• NIH Device Record Key: 22425828-1766-41f1-95e9-a4b7b5046dff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EXPRESS
• Version Model Number: 19930
• Company DUNS: 051798999
• Company Name: ATRIUM MEDICAL CORPORATION
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00650862199307 [Primary]
GS1	20650862199301 [Package]; Contains: 00650862199307; Package: [10 Units]; In Commercial Distribution

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: 2019-01-15
• Device Publish Date: 2015-09-24

On-Brand Devices [EXPRESS]

• 20650862199301: EXPRESS MINI 500 SUCTION BULB
• 20650862164002: EXPRESS MINI 500 DRAIN
• 20650862115219: EXPRESS, Dual Collection (Express Dry Seal Chest Drain)
• 20650862115165: EXPRESS II, BRU, SFP (Express Dry Seal Chest Drain - ATS)
• 20650862115158: EXPRESS II, Single Collection, SFP (Express Dry Seal Chest Drain)
• 20650862115141: EXPRESS DRAIN ,BRU, INLINE & ATS COMPATIBLE
• 20650862115134: EXPRESS DRAIN, SINGLE, INLINE & ATS COMPATIBLE