MEIJER 74-509

GUDID 10713733353943

Meijer Ultra Premium Automatic Arm Digital BP Monitor

MEIJER, INC.

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 10713733353943
• NIH Device Record Key: dcb2d2b6-2d0b-4af8-9ac7-57851d0ed587
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MEIJER
• Version Model Number: 74-509
• Catalog Number: 74-509
• Company DUNS: 006959555
• Company Name: MEIJER, 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: 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	00713733353946 [Primary]
GS1	10713733353943 [Package]; Contains: 30713733353947; Package: MASTER SHIPPER [12 Units]; In Commercial Distribution
GS1	30713733353947 [Package]; Contains: 00713733353946; Package: INTERMEDIATE [2 Units]; In Commercial Distribution

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-11-08
• Device Publish Date: 2018-08-31

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