MaxGuard MX1002
MaxGuard MX1002 is a medical device (FDA Class II; FDA product code FPA, Set, administration, intravascular) made by BD Switzerland Sàrl, listed in FDA GUDID since 22 Sep 2016 (UDI-DI 10885403237447), 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 | Number10885403237447 | Date22 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 10885403237447
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- MaxGuard
- Generic name
- Negative-pressure intravenous line needleless valve-connector
- Model / Ref / Catalog
- MX1002
- Primary DI / UDI-DI
- 10885403237447
- FDA product code
- FPA
- 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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