LensChekPro

GUDID 00812559012287

REICHERT, INC.

Automated lensmeter

• Primary Device ID: 00812559012287
• NIH Device Record Key: 94a02da9-2e5c-43e2-a56e-8d9d09e0f032
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LensChekPro
• Version Model Number: 15185
• Company DUNS: 126650253
• Company Name: REICHERT, 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: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812559012287 [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: 2025-08-20
• Device Publish Date: 2025-08-12

Devices Manufactured by REICHERT, INC.

• 00812559012485 - Ocu-Film® +": 2025-08-25
• 00812559012492 - Ocu-Film® +": 2025-08-22
• 00812559010238 - Ultramatic RX Master Phoropter: 2025-08-20
• 00812559010269 - Ultramatic RX Master Phoropter: 2025-08-20
• 00812559010290 - Illuminated Phoropter: 2025-08-20
• 00812559010320 - Illuminated Phoropter: 2025-08-20
• 00812559010559 - TF50 Trial Frame: 2025-08-20
• 00812559010566 - TS75 Trial Lens: 2025-08-20