Foster & Thrive

GUDID 10010939960181

MCKESSON CORPORATION

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• Primary Device ID: 10010939960181
• NIH Device Record Key: 1f0b5ce0-3298-4d63-9680-abcc1139964f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Foster & Thrive
• Version Model Number: BPAG1-20MFT(2878106)
• Company DUNS: 177667227
• Company Name: MCKESSON 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	00010939960184 [Primary]
GS1	10010939960181 [Package]; Contains: 00010939960184; Package: Box packing [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K221857

FDA Product Code

• DXQ: Blood Pressure Cuff

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-06-26
• Device Publish Date: 2024-06-18

On-Brand Devices [Foster & Thrive]

• 10010939960181: BPAG1-20MFT(2878106)
• 10010939960167: BP3NM1-3WMFT(2878080)