Alaris, SmartSite 2000EA
Alaris, SmartSite 2000EA is a medical device (FDA Class II) made by BD Switzerland Sàrl, listed in FDA GUDID since 22 Sep 2016 (UDI-DI 07613203012751), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07613203012751 | Date22 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 07613203012751
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Alaris, SmartSite
- Generic name
- Negative-pressure intravenous line needleless valve-connector
- Model / Ref / Catalog
- 2000EA
- Primary DI / UDI-DI
- 07613203012751
- FDA product code
- FPA, LHI
- GMDN term
- Negative-pressure intravenous line needleless valve-connector
- Device class
- Class II
- Regulation number
- 880.5440
- GUDID distribution status
- In Commercial Distribution
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