Schaumstoffkissen
by Bisanz medizinische Polster GmbH 132 variants
Ref 300089PUModel Universelle Lagerungskissen
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Overview
Schaumstoffkissen medical device directory provides an overview of the Bisanz medizinische Polster GmbH Schaumstoffkissen, including its features, compliance, and regulatory status. This device is designed for use in human anatomy and has undergone comprehensive testing.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number42519313UniverLHM3 04251931328510 | Date22 Apr 2026 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- Universelle Lagerungskissen, 300089PU
- Primary DI / UDI-DI
- 04251931328510
- Basic UDI-DI
- 42519313UniverLHM3
- EMDN Code
- V080302 Patient positioning medical cushions
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000006356
Other devices from Bisanz medizinische Polster GmbH
Properties
Other properties (13)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: 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