Merit Disposal Depot™ MDD220H/B

GUDID 20884450008236

Merit Medical Systems, Inc.

Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle

• Primary Device ID: 20884450008236
• NIH Device Record Key: 58ec314b-7781-4d7e-a744-b9248f1b1114
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Merit Disposal Depot™
• Version Model Number: 00884450008232
• Catalog Number: MDD220H/B
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• 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: false
• OTC Over-The-Counter: false

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450008232 [Primary]
GS1	10884450008239 [Package]; Contains: 00884450008232; Package: [20 Units]; In Commercial Distribution
GS1	20884450008236 [Package]; Contains: 10884450008239; Package: [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K914208

FDA Product Code

• DQO: CATHETER, INTRAVASCULAR, DIAGNOSTIC

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: 2016-09-26

On-Brand Devices [Merit Disposal Depot™]

• 10884450123130: 00884450123133
• 20884450050105: 00884450050101
• 20884450028579: 00884450028575
• 10884450024451: 00884450024454
• 20884450024403: 00884450024409
• 10884450023676: 00884450023679
• 20884450022850: 00884450022856
• 20884450022089: 00884450022085
• 20884450019607: 00884450019603
• 20884450013421: 00884450013427
• 20884450008236: 00884450008232
• 20884450008229: 00884450008225
• 10884450419769: 00884450419762
• 20884450504936: 00884450504932