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Footboard

FDA UDI

Class II (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Footboard FDA UDI
Generic Name
Basic electric home bed FDA UDI
Device Name
Footboard for D300 with 5 Function Staff Control, Light Oak FDA UDI
Model / Reference
12915-OA FDA UDI
Description
Footboard for D300 with 5 Function Staff Control, Light Oak FDA UDI

Identifiers

Primary DI / UDI-DI
00840117303461 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Basic electric home bed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5100 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: Basic electric home bed

Footboard by Dynarex Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic electric home bed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 122e899d-a374-41e6-bef9-9ead296865f6 33 fields · synced Jun 8, 2026