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PCG series

FDA UDI

Class I (US FDA UDI)

by Oakworks, Inc.

Identity

Trade Name
PCG series FDA UDI
Generic Name
Examination/treatment table, line-powered FDA UDI
Device Name
100 Procedure Chair 3 Section Top; 27" Width; 240V Electric FDA UDI
Model / Reference
100 Procedure Chair / PCG Chair FDA UDI
Description
100 Procedure Chair 3 Section Top; 27" Width; 240V Electric FDA UDI

Identifiers

Primary DI / UDI-DI
00817463026658 FDA UDI
FDA Product Code
LGX FDA UDI
GMDN Term
Examination/treatment table, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

PCG series by Oakworks, Inc. — 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
Oakworks, Inc.

Sources (1)

  • FDA UDI 9d7d10b3-bf94-4547-9208-20070e7fb5b9 34 fields · synced May 30, 2026