Clareon Vivity CNWET3
by Alcon Laboratories, Inc. 45 variants
Ref CNWET3-250
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number00380658454265 | Date3 Sep 2026 | StatusListed |
| European Union | CE/MDR EUDAMED | Number038065GMN000243H7 00380658454265 | Date3 Aug 2026 | StatusActive |
Certificates
- G70 020895 0414 Withdrawn
Technical documentation EU MDR
- Certifier
- TÜV SÜD Product Service GmbH 0123
- Issued
- 11 Jun 2026
- Expires
- 20 Jan 2030
- Reason
- Transferred to other nb
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Clareon Vivity
- Generic Name
- Posterior-chamber intraocular lens, pseudophakic
- Model / Ref / Catalog
- CNWET3-250, CNWET3
- Primary DI / UDI-DI
- 00380658454265
- Basic UDI-DI
- 038065GMN000243H7
- FDA Product Code
- POE
- EMDN Code
- P030102100301 IOLs, APHAKIC, MULTIFOCAL, TORIC, HYDROPHOBIC ACRYLIC
- GMDN Term
- Posterior-chamber intraocular lens, pseudophakic
- Device Class
- Class IIb EUDAMEDClass III GUDID
- Regulation Number
- 886.3600
- EU market of registration
- Belgium
- GUDID distribution status
- In Commercial Distribution
- MRI Safety
- MR Safe
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / Reference | CNWET3-250 | CNWET3 |
| Device Class | Class IIb | Class III |
Other devices from Alcon Laboratories, Inc.
Properties
Other properties (17)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Sutures: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No