Identity
- Trade Name
- SENSAR IOL FDA UDI
- Generic Name
- Posterior-chamber intraocular lens, pseudophakic FDA UDI
- Device Name
- AMO Sensar AR40e Lens FDA UDI
- Model / Reference
- AR40e FDA UDI
- Description
- AMO Sensar AR40e Lens FDA UDI
Identifiers
- Catalog Number
- AR40E00115 FDA UDI
- Primary DI / UDI-DI
- 05050474514157 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
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
Single Use
Yes
Implantable
Yes
Contains Latex
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
No
Serial Number
Yes
Expiration Date
Yes
Manufacturing Date
Yes
Dimensions & Sizes
- Size
- Outer Diameter — 13 Millimeter FDA UDI
Category: Posterior-chamber intraocular lens, pseudophakic
The Sensar IOL is a high-quality, post-cataract intraocular lens (IOL) designed for permanent implantation in the posterior chamber of the eye. This device features a unique, thin design and advanced optics for clear vision, while also being durable and resistant to wear. With its sterile, single-use or disposable design options, the Sensar IOL is an attractive solution for ophthalmic surgeons seeking to improve patient outcomes.
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Authorization Coverage (1 country)
Regulatory Authorizations
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
- Johnson & Johnson Surgical Vision, Inc.
Sources (1)
- FDA UDI fd5e5adb-6d8c-4cef-bcc8-2a1143f01082 37 fields · synced Jul 21, 2026