← Back to catalogue

Procedure Chair

FDA UDI

Class I (US FDA UDI)

by Oakworks, Inc.

Identity

Trade Name
Procedure Chair FDA UDI
Generic Name
General examination/treatment chair, electric FDA UDI
Device Name
3000 3 Section Top; 26" Width; 120V Electric FDA UDI
Model / Reference
3000 FDA UDI
Description
3000 3 Section Top; 26" Width; 120V Electric FDA UDI

Identifiers

Primary DI / UDI-DI
00817463027020 FDA UDI
FDA Product Code
LGX FDA UDI
GMDN Term
General examination/treatment chair, electric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 FDA UDI
Commercial Distribution
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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General examination/treatment chair, electric

Procedure Chair by Oakworks, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General examination/treatment chair, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Oakworks, Inc.

Sources (1)

  • FDA UDI a4d606c2-2014-400c-b885-705349fce043 33 fields · synced Jun 8, 2026