Imflex Light Body FS

GUDID 08800024201610

Sherpakorea

Silicone dental impression material

• Primary Device ID: 08800024201610
• NIH Device Record Key: 21dd7b28-d3a1-4720-82ba-f1482fed5319
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Imflex Light Body FS
• Version Model Number: Imflex Light Body Fast (50ml * 2 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	08800024201610 [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: 2020-04-16
• Device Publish Date: 2020-04-08

Devices Manufactured by Sherpakorea

• 08800024201986 - Implant Heavy Body: 2023-08-11
• 08800024205946 - Implant Monophase: 2023-08-11
• 08800024206011 - Implant Light Body: 2023-08-11
• 08800024206318 - Deli-Bite Clear: 2023-07-06
• 08800024206295 - Delikit Extra Light Body Fast: 2023-06-26
• 08800024206288 - Delikit Implant Heavy Body: 2023-06-07
• 08800024205793 - Delikit 7.0 Light Body Fast: 2023-06-02
• 08800024205885 - Delikit 7.0 Extra Light Body Fast: 2023-06-02