Sphygmomanometer

GUDID 00616784710839

DYNAREX CORPORATION

Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer

• Primary Device ID: 00616784710839
• NIH Device Record Key: 31235ec0-29f0-4dd6-89de-16b7c417e214
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sphygmomanometer
• Version Model Number: 7108
• Company DUNS: 008124539
• Company Name: DYNAREX 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00616784710815 [Primary]
GS1	00616784710839 [Package]; Contains: 00616784710815; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092245

FDA Product Code

• DXQ: Blood Pressure Cuff

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

On-Brand Devices [Sphygmomanometer]

• 00616784710938: 7109
• 00616784710839: 7108
• 00616784710730: 7107
• 00616784710631: 7106
• 00616784710532: 7105
• 00616784710433: 7104