CRYOTUBE 1.0 ml SI Internal Starfoot Conical

GUDID 25713311000193

CRYOTUBE 1.0 ml SI Internal Starfoot Conical is used for storage and transportation of biological material for in vitro Diagnostics.

Nunc A/S

General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium

• Primary Device ID: 25713311000193
• NIH Device Record Key: 0d80a618-4122-4470-baab-32105db026d2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CRYOTUBE 1.0 ml SI Internal Starfoot Conical
• Version Model Number: 377224
• Company DUNS: 305971764
• Company Name: Nunc A/S
• Device Count: 50
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	15713311000196 [Primary]
GS1	25713311000193 [Package]; Contains: 15713311000196; Package: PACK [10 Units]; In Commercial Distribution
GS1	35713311000190 [Package]; Package: CASE [4 Units]; In Commercial Distribution
GS1	85713311000195 [Unit of Use]

FDA Product Code

• FMH: Container, Specimen, Sterile

Sterilization

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

[25713311000193]

Radiation Sterilization

[25713311000193]

Radiation Sterilization

[25713311000193]

Radiation Sterilization

[25713311000193]

Radiation Sterilization

[25713311000193]

Radiation Sterilization

[25713311000193]

Radiation Sterilization

[25713311000193]

Radiation Sterilization

[25713311000193]

Radiation Sterilization

[25713311000193]

Radiation Sterilization

[25713311000193]

Radiation Sterilization

[25713311000193]

Radiation Sterilization

[25713311000193]

Radiation Sterilization

[25713311000193]

Radiation Sterilization

[25713311000193]

Radiation Sterilization

[25713311000193]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-10-18
• Device Publish Date: 2022-10-10

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