Protekt

FDA UDI

Class II (US FDA UDI)

by Proactive Medical Products

Identity

Trade Name: Protekt FDA UDI
Generic Name: Basic electric home bed FDA UDI
Device Name: Protekt Semi-Electric Bed, Spring Deck w/ Half Rails, 1pc /2ctn, with 9V battery FDA UDI
Model / Reference: PMSEBHR FDA UDI
Description: Protekt Semi-Electric Bed, Spring Deck w/ Half Rails, 1pc /2ctn, with 9V battery FDA UDI

Identifiers

Catalog Number: PMSEBHR FDA UDI
Primary DI / UDI-DI: 05060488573989 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Height — 24 Inch FDA UDI
Length — 80 Inch FDA UDI
Width — 36 Inch FDA UDI

Category: Basic electric home bed

Protekt by Proactive Medical Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Basic electric home bed.

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DRIVEMEDICAL — Drive Devilbiss Healthcare · Class II
Long Term Care Bed — Dynarex Corp. · Class II
Footboard — Dynarex Corp. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Proactive Medical Products

Sources (1)

FDA UDI a6b50052-ab99-4536-974b-ba7659e7212b 36 fields · synced Jun 6, 2026