Pasante Glow
by Karex Industries Sdn. Bhd. 2 variants
Ref R1230K, R0304K
Active
CE MDR CE MDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberB-05060493181438 | Date6 Mar 2026 | StatusActive |
| European Union | CE/MDD | NumberB-05060493181438 | Date6 Mar 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR, CE/MDD Active
Specification
- Device Name
- Non-sterile, Non-Medicated Natural Rubber Latex Male CondomNon-sterile, Non-medicated Natural Rubber Latex Male Condoms
- Model / Reference
- R1230K, R0304K
- Primary DI / UDI-DI
- 05060493181438, 05060150684265
- Basic UDI-DI
- B-05060493181438, B-05060150684265, 9556564-NMCM-U4
- EMDN Code
- U110101 Condoms
- Device Class
- Class IIb
- EU market of registration
- FranceIreland
Manufacturer details
- EUDAMED SRN
- MY-MF-000001247
- Authorised representative
- Advena Limited MT-AR-000000234
Other devices from Karex Industries Sdn. Bhd.
Properties
Other properties (12)
- Sterile: No
- Implantable: No
- Reusable: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No