PX Wave
by Shanwei Perfect Medical Instruments Co., Ltd. 6 variants
Ref Z497 201 903 2102 015Model ET Files、V BLUE、MTF、TG6、TH6、TF4 etc
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 | Number697590932NiTiRotary96 | Date23 Aug 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- Withdrawn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
- Dental Root-Canal Instruments
- Model / Reference
- ET Files、V BLUE、MTF、TG6、TH6、TF4 etc, Z497 201 903 2102 015
- Primary DI / UDI-DI
- 06942200937479, 06942200937509, 06942200922888, 06942200922895
- Basic UDI-DI
- 697590932NiTiRotary96
- EMDN Code
- Q010507 Endodontic instruments (canal enlargers, files, rasps, etc.), single-use
- Device Class
- Class IIa
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000033003
- Authorised representative
- SUNGO Europe B.V. NL-AR-000000247
Other devices from Shanwei Perfect Medical Instruments Co., Ltd.
See all devices from Shanwei Perfect Medical Instruments Co., Ltd. →
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