Pinnacle® 2112431
Pinnacle® 2112431 is a Class II device made by B. Braun Medical, Inc., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04046964201141), registry data as of 22 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 | Number04046964201141 | Date23 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 04046964201141
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Pinnacle®
- Generic name
- Compounding transfer set
- Model / Ref / Catalog
- 2112431
- Primary DI / UDI-DI
- 04046964201141
- FDA product code
- KPE, LHI
- GMDN term
- Compounding transfer set
- Device class
- Class II
- Regulation number
- 880.5025, 880.5440
- GUDID distribution status
- In Commercial Distribution
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