Mani Sutures Polypropylene - 10-0 Polypropylene
Ref 1460P
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-04546951401535 | Date30 Oct 2025 | StatusActive |
| European Union | CE/MDD | NumberB-04546951401535 | Date30 Oct 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- Withdrawn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, CE/MDD Active
Specification
- Device Name
- Mani Sutures Polypropylene
- Model / Reference
- 1460P
- Primary DI / UDI-DI
- 04546951401535, 04546951633943
- Basic UDI-DI
- B-04546951401535, 4546951000005ZH
- EMDN Code
- H010201010401 Polypropylene monofilament with needle for open surgery
- Device Class
- Class IIb
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- JP-MF-000017860
- Authorised representative
- Obelis s.a. BE-AR-000000106
Other devices from Mani, Inc.
Properties
Other properties (10)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No