Single Mirror Kaufman Laser Lens

GUDID 00630238007092

OCULAR INSTRUMENTS, INC.

Gonioscope

• Primary Device ID: 00630238007092
• NIH Device Record Key: 7cebdecd-c701-4832-8f52-a1fc8cd8309b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Single Mirror Kaufman Laser Lens
• Version Model Number: OKSMA
• Company DUNS: 046212387
• Company Name: OCULAR INSTRUMENTS, INC.
• 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: false
• 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	00630238007092 [Primary]

FDA Product Code

• HKS: Prism, Gonioscopic

Sterilization

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

[00630238007092]

High-level Disinfectant

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-06-20
• Device Publish Date: 2019-06-12

Devices Manufactured by OCULAR INSTRUMENTS, INC.

• 00630238081795 - MaxLight® Standard 90D Slit Lamp Indirect Lens (Green): 2021-03-17
• 00630238007122 - Ritch Trabeculoplasty Laser Lens: 2020-02-19
• 00630238122245 - 13063 RxSight 0.766x Mag Contact Lens: 2019-09-19
• 00630238084741 - MaxAC® Lens Stand: 2019-09-10
• 00063023800712 - Ritch Trabeculoplasty Laser Lens: 2019-06-20
• 00630238006972 - Koeppe Extra Small Diagnostic Lens 12mm O.D.: 2019-06-20
• 00630238007092 - Single Mirror Kaufman Laser Lens: 2019-06-20
• 00630238007092 - Single Mirror Kaufman Laser Lens: 2019-06-20
• 00630238008075 - Koeppe Large Diagnostic Lens 19mm O.D.: 2019-06-20