CoreBloc SK820000

GUDID 27350081910093

Prostalund AB

Percutaneous medicine administration kit, non-medicated, single-use

• Primary Device ID: 27350081910093
• NIH Device Record Key: 9bcd5b99-4370-4f4e-b080-8e8fb72cfc4f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CoreBloc
• Version Model Number: SK820000
• Catalog Number: SK820000
• Company DUNS: 554703897
• Company Name: Prostalund AB
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07350081910099 [Primary]
GS1	27350081910093 [Package]; Contains: 07350081910099; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• GAA: Needle, Aspiration And Injection, Disposable

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-07-06
• Device Publish Date: 2018-06-05

Devices Manufactured by Prostalund AB

• 07350081910013 - CoreTherm: 2018-07-06
• 07350081910020 - CoreTherm: 2018-07-06
• 07350081910037 - CoreTherm: 2018-07-06
• 07350081910044 - CoreTherm: 2018-07-06
• 07350081910051 - CoreTherm: 2018-07-06
• 07350081910068 - CoreTherm: 2018-07-06
• 07350081910075 - CoreTherm: 2018-07-06
• 07350081910082 - CoreTherm: 2018-07-06