Dlp® 10003
Dlp 10003 is a cardioplegia solution administration adaptor (FDA Class II; FDA product code DTL, Adaptor, stopcock, manifold, fitting, cardiopulmonary bypass) made by Medtronic, Inc., listed in FDA GUDID since 22 May 2016 (UDI-DI 20613994808022), 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 | Number20613994808022 | Date22 May 2016 | StatusListed |
Official records
- AccessGUDID record 20613994808022
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Dlp®
- Generic name
- Cardioplegia solution administration adaptor
- Model / reference
- 10003
- Primary DI / UDI-DI
- 20613994808022
- FDA product code
- DTL
- GMDN term
- Cardioplegia solution administration adaptor
- Device class
- Class II
- Regulation number
- 870.4290
- GUDID distribution status
- In Commercial Distribution
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