Planmeca Chair
by Planmeca Oy
Planmeca Chair (10026000) is a Class I device made by Planmeca Oy, listed in FDA GUDID since 8 May 2017 (UDI-DI 06430035420162), not in commercial distribution (GUDID) as of 21 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 | Number06430035420162 | Date8 May 2017 | StatusListed |
Official records
- AccessGUDID record 06430035420162
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Dental chair, electric
- Model / Ref / Catalog
- Chair, 10026000
- Primary DI / UDI-DI
- 06430035420162
- FDA product code
- KLC
- GMDN term
- Dental chair, electric
- Device class
- Class I
- Regulation number
- 872.6250
- GUDID distribution status
- Not in Commercial Distribution
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