MaxLight® Standard 90D Slit Lamp Indirect Lens (Green)

GUDID 00630238081979

OCULAR INSTRUMENTS, INC.

Diagnostic condensing lens

• Primary Device ID: 00630238081979
• NIH Device Record Key: 18a71dfe-ddbc-47a8-aa36-4a6f02cf5f70
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MaxLight® Standard 90D Slit Lamp Indirect Lens (Green)
• Version Model Number: OI-STD/GN
• 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	00630238081979 [Primary]

FDA Product Code

• HJL: Lens, Condensing, Diagnostic

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: 2019-06-19
• Device Publish Date: 2019-06-11

On-Brand Devices [MaxLight® Standard 90D Slit Lamp Indirect Lens (Green)]

• 00630238081979: OI-STD/GN
• 00630238081795: OI-STD/GN