Microclear

GUDID 06970990160104

Suzhou Microclear Medical Instruments Co., Ltd.

External ocular measurement camera

• Primary Device ID: 06970990160104
• NIH Device Record Key: b532051a-507c-4ad8-99f9-a932000d35db
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Microclear
• Version Model Number: VS
• Company DUNS: 548374439
• Company Name: Suzhou Microclear Medical Instruments 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: true
• Serial Number: true
• Manufacturing Date: true
• 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	06970990160104 [Primary]

FDA Product Code

• HKO: Refractometer, Ophthalmic

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: 2021-02-04
• Device Publish Date: 2021-01-27

On-Brand Devices [Microclear]

• 06970990160159: VS-T Plus
• 06970990160142: VS-T Pro
• 06970990160135: VS-T
• 06970990160128: VS-Plus
• 06970990160111: VS-Pro
• 06970990160104: VS
• 06970990160098: HSL-03
• 06970990160081: HSL-02
• 06970990160074: HSL-01
• 06970990160067: FC-03
• 06970990160050: FC-02
• 06970990160043: FC-01
• 06970990160029: HSL
• 06970990160012: HFC