Redpine Rp-U-P1502
by Guangzhou Red Pine Medical Instrument Co., Ltd.
Redpine Rp-U-P1502 is a Class I device made by Guangzhou Red Pine Medical Instrument Co., Ltd., listed in FDA GUDID since 25 Aug 2023 (UDI-DI 06972520300943), 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 | Number06972520300943 | Date25 Aug 2023 | StatusListed |
Official records
- AccessGUDID record 06972520300943
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Redpine
- Generic name
- Rigid endoscopic biopsy forceps, single-use
- Model / reference
- RP-U-P1502
- Primary DI / UDI-DI
- 06972520300943
- FDA product code
- FCL
- GMDN term
- Rigid endoscopic biopsy forceps, single-use
- Device class
- Class I
- Regulation number
- 876.1075
- GUDID distribution status
- In Commercial Distribution
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