Kerator Cap

GUDID 08809488213320

KJMEDITECH.CO.,LTD

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 08809488213320
• NIH Device Record Key: c881952b-d1b5-47d1-be31-c3a6a117ba53
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kerator Cap
• Version Model Number: CPR2
• Company DUNS: 688476027
• Company Name: KJMEDITECH.CO.,LTD
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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	08809488213320 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132144

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[08809488213320]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-11-08
• Device Publish Date: 2019-08-28

On-Brand Devices [Kerator Cap]

• 08809488213344: CPB2
• 08809488213337: CPP2
• 08809488213320: CPR2
• 08809488213313: CPD2