SupraSperm

GUDID 00888937801224

SupraSperm 100%. 500 ml

Origio A/S

IVF medium

• Primary Device ID: 00888937801224
• NIH Device Record Key: 4f64f3fe-c524-49e4-8530-1ed4bc7d9d3e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SupraSperm
• Version Model Number: 10970500D
• Company DUNS: 305424269
• Company Name: Origio A/S
• 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: true
• 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

• Storage Environment Temperature: Between 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888937801224 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K003404

FDA Product Code

• MQL: Media, Reproductive

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-15

On-Brand Devices [SupraSperm]

• 20888937801198: SupraSperm 100. 2x60 ml
• 00888937801224: SupraSperm 100%. 500 ml