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Planmeca Chair

FDA UDI

Class I (US FDA UDI)

by Planmeca Oy

Identity

Trade Name
Planmeca Chair FDA UDI
Generic Name
Dental chair, electric FDA UDI
Device Name
Planmeca Chair is electronically controlled patient chair with swivel funcion allowing the chair to be swivelled 90 degrees to left and right. The chair has an integrated foot control for automatic chair positions and manual movements. The chair can be equipped with optional foldable knee-break. FDA UDI
Model / Reference
Chair FDA UDI
Description
Planmeca Chair is electronically controlled patient chair with swivel funcion allowing the chair to be swivelled 90 degrees to left and right. The chair has an integrated foot control for automatic chair positions and manual movements. The chair can be equipped with optional foldable knee-break. FDA UDI

Identifiers

Catalog Number
10026000 FDA UDI
Primary DI / UDI-DI
06430035420162 FDA UDI
FDA Product Code
KLC FDA UDI
GMDN Term
Dental chair, electric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6250 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Planmeca Chair by Planmeca Oy — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Planmeca Oy

Sources (1)

  • FDA UDI 0346cf77-4329-45ca-9373-05887c200dbb 35 fields · synced May 30, 2026