HemoCue® Hb 201+ Analyzer 121720

GUDID 07311091217202

HemoCue Hb 201+ Analyzer g/L

Hemocue AB

Haemoglobin analyser IVD, point-of-care

• Primary Device ID: 07311091217202
• NIH Device Record Key: 0b549fdd-7ef4-4e1b-af4f-3af8c03f7385
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HemoCue® Hb 201+ Analyzer
• Version Model Number: 121720
• Catalog Number: 121720
• Company DUNS: 356164426
• Company Name: Hemocue AB
• 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

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *The analyzer should not be stored at high (i.e. >90% non-condensing) humidity
• Storage Environment Temperature: Between 32 Degrees Fahrenheit and 122 Degrees Fahrenheit
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	07311091217202 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K032203

FDA Product Code

• GKR: System, Hemoglobin, Automated

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: 2016-05-31

On-Brand Devices [HemoCue® Hb 201+ Analyzer]

• 07311091217219: HemoCue Hb 201+ Analyzer g/dL
• 07311091217202: HemoCue Hb 201+ Analyzer g/L