CROWNJUN Micro Sheet K 0KM01

GUDID 04946585290992

KONO SEISAKUSHO CO.,LTD.

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• Primary Device ID: 04946585290992
• NIH Device Record Key: eca514f8-d51b-4114-be0e-66b1c73aeb42
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CROWNJUN Micro Sheet K
• Version Model Number: 0KM01
• Catalog Number: 0KM01
• Company DUNS: 691486468
• Company Name: KONO SEISAKUSHO CO.,LTD.
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04946585290992 [Primary]
GS1	14946585290999 [Package]; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• FTY: Tape, Measuring, Rulers And Calipers

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: 2023-03-22
• Device Publish Date: 2023-03-14

Devices Manufactured by KONO SEISAKUSHO CO.,LTD.

• 14946585346436 - CROWNJUN Nylon Suture: 2024-04-09
• 04946585348464 - CROWNJUN Nylon Suture: 2024-04-09
• 04946585324079 - PICOCLAMP: 2023-11-22
• 14946585324083 - PICOCLAMP: 2023-11-22
• 14946585324090 - PICOCLAMP: 2023-11-22
• 14946585324106 - PICOCLAMP: 2023-11-22
• 14946585324113 - PICOCLAMP: 2023-11-22
• 14946585324120 - PICOCLAMP: 2023-11-22