Identity
- Trade Name
- AcrySof® FDA UDI
- Generic Name
- Posterior-chamber intraocular lens, pseudophakic FDA UDI
- Device Name
- AcrySof® Aspheric UV Absorbing Toric Posterior Chamber Intraocular Lens (IOL) FDA UDI
- Model / Reference
- SA6AT8 FDA UDI
- Description
- AcrySof® Aspheric UV Absorbing Toric Posterior Chamber Intraocular Lens (IOL) FDA UDI
Identifiers
- Catalog Number
- SA6AT8U300 FDA UDI
- Primary DI / UDI-DI
- 00380652362313 FDA UDI
- FDA Product Code
- HQL FDA UDI
- GMDN Term
- Posterior-chamber intraocular lens, pseudophakic FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Regulation Number
- 886.3600 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
AcrySof is a high-quality, aspheric UV-absorbing toric intraocular lens (IOL) designed to enhance vision and reduce dependence on glasses or contact lenses in patients with astigmatism.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Alcon Laboratories, Inc.
Sources (1)
- FDA UDI 8c831d03-98dc-4a1f-92ff-516d367fbbd4 37 fields · synced Jul 25, 2026