PlumePort SEV
by Buffalo Filter Co., Inc. GUDID
Withdrawn
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00851136002587 | Date13 Jan 2017 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- Trade Name
- PlumePort
- Generic Name
- Surgical plume evacuation system tube
- Model / Ref / Catalog
- SEV, BLAP100V
- Primary DI / UDI-DI
- 00851136002587
- FDA Product Code
- NKC
- GMDN Term
- Surgical plume evacuation system tube
- Device Class
- Class I
- Regulation Number
- 884.1730
- Commercial Distribution
- Not in Commercial Distribution
Other devices from Buffalo Filter Co., Inc.
Properties
Other properties (8)
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Manufacturing Date: No