Identity
- Trade Name
- AcrySof® IQ ReSTOR® FDA UDI
- Generic Name
- Posterior-chamber intraocular lens, pseudophakic FDA UDI
- Device Name
- AcrySof® IQ ReSTOR® MultiFocal Toric IOL, UV w/ Blue Light Filter, PC Lens, 13.0mm Length, 6.0mm Biconvex Optic, Planar Haptics FDA UDI
- Model / Reference
- SV25T5 FDA UDI
- Description
- AcrySof® IQ ReSTOR® MultiFocal Toric IOL, UV w/ Blue Light Filter, PC Lens, 13.0mm Length, 6.0mm Biconvex Optic, Planar Haptics FDA UDI
Identifiers
- Catalog Number
- SV25T5U235 FDA UDI
- Primary DI / UDI-DI
- 00380652312752 FDA UDI
- FDA Product Code
- MFK 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® IQ ReSTOR® by Alcon Laboratories, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Alcon Laboratories, Inc.
Sources (1)
- FDA UDI 4856ae39-46d9-429e-9f59-57868c555105 37 fields · synced Jun 8, 2026