Delikit Bite Registration

GUDID 08800024201573

Sherpakorea

Silicone dental impression material

• Primary Device ID: 08800024201573
• NIH Device Record Key: 40e42025-cd08-4937-9e85-641a6b22cffe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Delikit Bite Registration
• Version Model Number: Delikit Bite Registration (50ml * 200 Cartridges)
• Company DUNS: 557822311
• Company Name: Sherpakorea
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +827078429961
• Email: happidenco@naver.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800024201573 [Primary]

FDA Product Code

• ELW: Material, Impression

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-03-24
• Device Publish Date: 2020-03-16

On-Brand Devices [Delikit Bite Registration]

• 08800024201573: Delikit Bite Registration (50ml * 200 Cartridges)
• 08800024201535: Delikit Bite Registration (50ml * 50 Cartridges)
• 08800024201894: Delikit Bite Registration (50ml * 4 Cartridges)
• 08800024203232: Delikit Bite Registration (50ml * 10 Cartridges)