enVista MX60 IOL
- Primary DI
- 10757770548191
- Brand
- enVista MX60 IOL
- Company
- Bausch & Lomb Incorporated
- Model
- MXUPT090+145
- Catalog number
- MXUPT090+145
- Device description
- MX60UPT090 12.5MM +14.5
- Published
- 2020-07-17
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes
| Code | Name |
|---|
| NAA | Lens, Intraocular, Accommodative |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| NAA | Lens, Intraocular, Accommodative | Ophthalmic | 3 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 10757770548191 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|
| 10757770548191 | 10757770548191 |
GMDN Terms
| Term | Definition |
|---|
| Posterior-chamber intraocular lens, pseudophakic | An optical device, generally referred to as an intraocular lens (IOL), intended to be implanted permanently in the posterior chamber of the eye (ring-like space filled with aqueous humor between the iris, the crystalline lens, and the ciliary body) to replace the natural lens (crystalline lens), typically because it has been clouded by a cataract. The device is made of a synthetic material (e.g., plastic, hydrogel). Included may be a sterile, single-use, IOL injector into which this device is preloaded and ready for insertion into the eye. |
Regulatory Flags
- DUNS number
- 196603781
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- false
- Serial number
- true
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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