HAI Hook

GUDID 00852194002076

Hook, Surgical instrument for ophthalmic use

Hightech American Industrial Labs Inc

Eye muscle hook, reusable

• Primary Device ID: 00852194002076
• NIH Device Record Key: 57d607e8-eb02-4ada-b64b-2be0d3453a6d
• Commercial Distribution Discontinuation: 2025-12-15
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: HAI Hook
• Version Model Number: 1
• Company DUNS: 961991916
• Company Name: Hightech American Industrial Labs Inc
• Device Count: 1
• DM Exempt: true
• 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: 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	00852194002076 [Primary]

FDA Product Code

• HNQ: Hook, Ophthalmic

Sterilization

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

[00852194002076]

Dry Heat Sterilization

[00852194002076]

Dry Heat Sterilization

[00852194002076]

Dry Heat Sterilization

[00852194002076]

Dry Heat Sterilization

[00852194002076]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-12-23
• Device Publish Date: 2025-12-15

Devices Manufactured by Hightech American Industrial Labs Inc

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• 00852194002014 - HAI CL-1000xyz clinical specular microscope: 2025-03-31 HAI CL-1000xyz is the clinical contact specular microscope. It evaluates the patient cornea endothelial cell layer. It is Clas