Merit Advance®

GUDID 10884450009052

Merit Medical Systems, Inc.

Anaesthesia conduction catheter holder, sterile

• Primary Device ID: 10884450009052
• NIH Device Record Key: d09938c3-5965-429c-9f4e-5cc849e0f1a0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Merit Advance®
• Version Model Number: 00884450009055
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, 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: 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 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 Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450009055 [Primary]
GS1	10884450009052 [Package]; Contains: 00884450009055; Package: [25 Units]; In Commercial Distribution
GS1	20884450009059 [Package]; Package: [4 Units]; In Commercial Distribution

FDA Product Code

• DRC: Trocar

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-24

On-Brand Devices [Merit Advance®]

• 10884450249151: 00884450249154
• 10884450151836: 00884450151839
• 10884450151812: 00884450151815
• 20884450151796: 00884450151792
• 10884450151775: 00884450151778
• 10884450151751: 00884450151754
• 10884450032012: 00884450032015
• 10884450031985: 00884450031988
• 10884450031978: 00884450031971
• 10884450031893: 00884450031896
• 10884450031800: 00884450031803
• 10884450031749: 00884450031742
• 10884450018184: 00884450018187
• 10884450017989: 00884450017982
• 20884450017924: 00884450017920
• 10884450017231: 00884450017234
• 10884450017194: 00884450017197
• 10884450016845: 00884450016848
• 10884450016838: 00884450016831
• 20884450016606: 00884450016602
• 20884450016583: 00884450016589
• 10884450015695: 00884450015698
• 10884450015688: 00884450015681
• 10884450010614: 00884450010617
• 10884450009090: 00884450009093
• 20884450009080: 00884450009086
• 20884450009073: 00884450009079
• 10884450009069: 00884450009062
• 10884450009052: 00884450009055
• 10884450009045: 00884450009048
• 20884450009035: 00884450009031
• 10884450009021: 00884450009024
• 20884450009011: 00884450009017
• 10884450009007: 00884450009000
• 10884450008994: 00884450008997
• 20884450008984: 00884450008980
• 10884450008970: 00884450008973
• 20884450008960: 00884450008966
• 20884450008199: 00884450008195
• 20884450008182: 00884450008188
• 20884450008175: 00884450008171
• 20884450412705: Initial Release
• 20884450151857: 10884450151850
• 20884450830776: B