Air-Flow-Piezon Dw-048A
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 | Number07613353171582 | Date13 Jul 2026 | 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- Withdrawn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
- Electromechanical device/system transport trolley
- Model / Ref / Catalog
- DW-048A
- Primary DI / UDI-DI
- 07613353171582
- 510(k) Number
- FDA Product Code
- EJR
- GMDN Term
- Electromechanical device/system transport trolley
- Device Class
- Class I
- Regulation Number
- 872.6030
- GUDID distribution status
- In Commercial Distribution
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