BlastFreeze

GUDID 60888937800571

BlastFreeze. 2x10 ml

Origio A/S

IVF medium kit

• Primary Device ID: 60888937800571
• NIH Device Record Key: a6b4ea6a-0fbb-497d-abbd-a552cf0904d6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BlastFreeze
• Version Model Number: 10532010D
• 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: true
• Device Combination Product: false
• Single Use: true
• 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

• Special Storage Condition, Specify: Between 0 and 0 *Protect from light
• Storage Environment Temperature: Between 2 Degrees Celsius and 8 Degrees Celsius
• Special Storage Condition, Specify: Between 0 and 0 *Protect from light
• Storage Environment Temperature: Between 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	60888937800571 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K031486

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: 2017-03-28

On-Brand Devices [BlastFreeze]

• 60888937816220: BlastFreeze. 4x2 ml
• 60888937800571: BlastFreeze. 2x10 ml