Max Fortis
by Terang Nusa (Malaysia) Sdn. Bhd. 6 variants
Ref MF-507611146, MF-507611148, MF-507611463, MF-507611141, MF-507611147, MF-507611144, MF-507611464, MF-507611462, MF-507611461, MF-507611468, MF-507611467
Active
CE MDR
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 | Number955507611080H7 | Date21 May 2025 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Sterile Latex Surgical Powder Free GloveSterile Latex Surgical Powdered Glove
- Model / Reference
- MF-507611146, MF-507611148, MF-507611463, MF-507611141, MF-507611147, MF-507611144, MF-507611464, MF-507611462, MF-507611461, MF-507611468, MF-507611467
- Primary DI / UDI-DI
- 09555076111460, 09555076111484, 09555076114638, 09555076111415, 09555076111477, 09555076111446, 09555076114645, 09555076114621, 09555076114614, 09555076114683, 09555076114676
- Basic UDI-DI
- 955507611080H7, 955507611000GF
- EMDN Code
- T01010102, T01010101
- Device Class
- Class IIa
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- MY-MF-000023462
- Authorised representative
- Ulma International GmbH DE-AR-000010015
Other devices from Terang Nusa (Malaysia) Sdn. Bhd.
Properties
Other properties (11)
- 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