Halo Sectional Matrix System 9932
Ref 9932
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number00883205044624 | Date26 Jun 2026 | StatusListed |
| European Union | CE/MDR EUDAMED | Number0883205-TF338BK 00883205044624 | Date9 Apr 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Halo Sectional Matrix System
- Generic Name
- Dental matrix band kit
- Device Name
- Halo
- Model / Ref / Catalog
- 9932
- Primary DI / UDI-DI
- 00883205044624
- Basic UDI-DI
- 0883205-TF338BK
- FDA Product Code
- JEP
- EMDN Code
- Q01010401 Paper and gutta-percha tips, matrices and wedges for dentistry
- GMDN Term
- Dental matrix band kit
- Device Class
- Class I
- Regulation Number
- 872.4565
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Ultradent Products, Inc.
Properties
Other properties (19)
- Sterile: No
- Single Use: 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
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No