Supracor Stimulite Honeycomb SMRT1817
by Supracor, Inc. GUDID
Withdrawn
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00842749103174 | Date27 Jul 2022 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- Trade Name
- Supracor Stimulite Honeycomb
- Generic Name
- Wheelchair seat cushion
- Model / Reference
- SMRT1817
- Primary DI / UDI-DI
- 00842749103174
- FDA Product Code
- IMP
- GMDN Term
- Wheelchair seat cushion
- Device Class
- Class I
- Regulation Number
- 890.3920
- Commercial Distribution
- Not in Commercial Distribution
Properties
Other properties (9)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No