BD MaxPlus MP2000
BD MaxPlus MP2000 is a Class II device made by BD Switzerland Sàrl, listed in FDA GUDID since 22 Sep 2016 (UDI-DI 10885403236532), 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 | Number10885403236532 | Date22 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 10885403236532
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- BD MaxPlus
- Generic name
- Intravenous administration tubing extension set
- Model / Ref / Catalog
- MP2000
- Primary DI / UDI-DI
- 10885403236532
- FDA product code
- FPA
- GMDN term
- Intravenous administration tubing extension set
- Device class
- Class II
- Regulation number
- 880.5440
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 7 Inch
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