gudid
Primary ID: 200
Acuity (UDI 200)
Manufactured by ACUITY POLYMERS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Acuity - Primary ID 200
Device Regulatory Overview
The Acuity (Model/Catalog Number: 200) is a medical device manufactured by ACUITY POLYMERS, INC.. This product is indexed under FDA Product Code / Category Classification HQD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 200
- Product Code / EMDN
- HQD
- Device Name
- Rigid-gas-permeable contact lens - daily wearfluoroxyfocon A
- Database Sync Date
- 2026-08-09 09:49:40
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Acuity?
The registered manufacturer of record for Acuity is ACUITY POLYMERS, INC..
What is the Primary UDI-DI identifier for Acuity?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 200.
What classification code is assigned to this device?
This device is registered under product classification code HQD.
Similar Classification Devices (HQD)
Other Devices by ACUITY POLYMERS, INC.
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