Plastcare RIT-5015
Plastcare RIT-5015 is a Class I device made by Plastcare USA, listed in FDA GUDID since 11 Mar 2020 (UDI-DI D915RIT50151), 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 | NumberD915RIT50151 | Date11 Mar 2020 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Plastcare
- Generic name
- Medicine cup, single-use
- Model / reference
- RIT-5015
- Primary DI / UDI-DI
- D915RIT50151
- FDA product code
- KYX
- GMDN term
- Medicine cup, single-use
- Device class
- Class I
- Regulation number
- 880.6430
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
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