Exacta Finger Pulse Oximeter

GUDID 10768627870310

Exacta Finger Pulse Oximeter

NORTH COAST MEDICAL, INC.

Pulse oximeter, battery-powered

• Primary Device ID: 10768627870310
• NIH Device Record Key: cbb478ca-aa24-4f14-839f-37f485bcd631
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Exacta Finger Pulse Oximeter
• Version Model Number: NC87031
• Company DUNS: 060121928
• Company Name: NORTH COAST MEDICAL, 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00768627870313 [Primary]
GS1	10768627870310 [Package]; Contains: 00768627870313; Package: Case [50 Units]; In Commercial Distribution

FDA Product Code

• DQA: Oximeter

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: 2018-03-29
• Device Publish Date: 2016-09-01

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