Puri Clear 500ml
Puri Clear 500ml is a Class IIa device made by Carl Zeiss Meditec AG, registered in EUDAMED on 27 Jul 2026 (Basic UDI-DI 4049336_P07_M09_R2A_65) with CE/MDR certificate 1000335292 valid until 5 Jan 2027, expiring as of 22 Oct 2026.
Expiring
CE MDR
Valid until
5 Jan 2027
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number1000335292 | Date16 Sep 2026 | StatusExpiring |
Official records
- EUDAMED public site 4049336_P07_M09_R2A_65
Certificates
- 1000335292 Expiring
Quality management system EU MDR
- Certifier
- DQS Medizinprodukte GmbH 0297
- Issued
- 16 Sep 2026
- Expires
- 5 Jan 2027
- Reason
- Add device or group
- 1000335292 Expiring
Quality management system EU MDR
- Certifier
- DQS Medizinprodukte GmbH 0297
- Issued
- 16 Sep 2026
- Expires
- 5 Jan 2027
- Reason
- Change approved
Timeline
- Registered EUDAMED 4049336_P07_M09_R2A_65
- Certificate issued EUDAMED 1000335292
- Certificate expires EUDAMED 1000335292
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Expiring
Specification
- Device name
- Puri Clear
- Primary DI / UDI-DI
- 04049336540466
- Basic UDI-DI
- 4049336_P07_M09_R2A_65
- Unit of use DI
- 04049336439371
- EMDN code
- Q02030203 Ophthalmic surgery balanced saline solutions
- Device class
- Class IIa
- EU registration type
- Standard device
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000007732
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