Air-Flow-Piezon Ft-229-2B-V02
by E.M.S. Electro Medical Systems S.A. 2 variants
Listed
Valid until
Not applicable
FDA recalls
3 ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07613353257323 | Date20 Oct 2025 | StatusListed |
Recalls
-
- Ongoing Z-1686-2024
- Ongoing Z-1687-2024
- Ongoing Z-1688-2024
Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles).
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Air-Flow-Piezon
- Generic Name
- Chairside dental abrasive air jet system
- Model / Reference
- FT-229-2B-V02
- Primary DI / UDI-DI
- 07613353257323
- 510(k) Number
- FDA Product Code
- ELC
- GMDN Term
- Chairside dental abrasive air jet system
- Device Class
- Class II
- Regulation Number
- 872.4850
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Electro Medical Systems (Ems Sa)
Properties
Other properties (11)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No
- Expiration Date: No