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Powerline

FDA UDI

Class I (US FDA UDI)

by Oakworks, Inc.

Identity

Trade Name
Powerline FDA UDI
Generic Name
Examination/treatment table, line-powered FDA UDI
Device Name
Powerline Flat Top Exam Table 1 Section Top; 24" Width FDA UDI
Model / Reference
Powerline Flat Top Exam Table FDA UDI
Description
Powerline Flat Top Exam Table 1 Section Top; 24" Width FDA UDI

Identifiers

Primary DI / UDI-DI
00817463026580 FDA UDI
FDA Product Code
KMN FDA UDI
GMDN Term
Examination/treatment table, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6140 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: Examination/treatment table, line-powered

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

Similar devices

Also classified as Examination/treatment table, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oakworks, Inc.

Sources (1)

  • FDA UDI b9001506-cc08-46cd-a2b0-93159e405dc0 33 fields · synced Jun 1, 2026