ProPlan CMF SD900.263
ProPlan CMF SD900.263 is a custom-made organ/bone anatomy model (FDA Class I; FDA product code HWT, Template) made by Materialise NV, listed in FDA GUDID since 13 Sep 2016 (UDI-DI 05420060352638), 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 | Number05420060352638 | Date13 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 05420060352638
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- ProPlan CMF
- Generic name
- Custom-made organ/bone anatomy model
- Model / Ref / Catalog
- SD900.263
- Primary DI / UDI-DI
- 05420060352638
- FDA product code
- HWT
- GMDN term
- Custom-made organ/bone anatomy model
- Device class
- Class I
- Regulation number
- 888.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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