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Overbed Table with U-Base

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Overbed Table with U-Base FDA UDI
Generic Name
Overbed table FDA UDI
Device Name
Overbed Table with U-Base, Amber Cherry and White, 32"x16", Adjustable Height 28" to 43" FDA UDI
Model / Reference
10453 FDA UDI
Description
Overbed Table with U-Base, Amber Cherry and White, 32"x16", Adjustable Height 28" to 43" FDA UDI

Identifiers

Primary DI / UDI-DI
00616784045313 FDA UDI
FDA Product Code
KMN FDA UDI
GMDN Term
Overbed table 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Overbed table

Overbed Table with U-Base by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Overbed table.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 7115f3c0-7f52-48f1-bfba-a632a0814767 33 fields · synced Jun 6, 2026