Lensmeter

GUDID 06973211070688

It is mainly used to measure the vertex power and prism power of various spectacle lenses, determine the position and direction of the column lens axis, print marks on the unprocessed lens, and check whether the lens are correctly installed in the frame

CHONGQING SUNKINGDOM MEDICAL INSTRUMENT CO.,LTD

Automated lensmeter

• Primary Device ID: 06973211070688
• NIH Device Record Key: 52745e92-13b1-40a7-be21-a8778ba8c9b7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lensmeter
• Version Model Number: SK-1000A
• Company DUNS: 545824560
• Company Name: CHONGQING SUNKINGDOM MEDICAL INSTRUMENT 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06973211070688 [Primary]

FDA Product Code

• HLM: Instrument, Measuring, Lens, Ac-Powered

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: 2020-07-10
• Device Publish Date: 2020-07-02

On-Brand Devices [Lensmeter]

• 06973211070695: It is mainly used to measure the vertex power and prism power of various spectacle lenses, deter
• 06973211070688: It is mainly used to measure the vertex power and prism power of various spectacle lenses, deter