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Protekt Supreme Support

FDA UDI

Class II (US FDA UDI)

by Proactive Medical Products

Identity

Trade Name
Protekt Supreme Support FDA UDI
Generic Name
Alternating-pressure bed mattress overlay system FDA UDI
Device Name
Protekt Supreme Support Non-Powered Self Adjusting Air/Foam Mattress System 60"x80"x7" FDA UDI
Model / Reference
94006 FDA UDI
Description
Protekt Supreme Support Non-Powered Self Adjusting Air/Foam Mattress System 60"x80"x7" FDA UDI

Identifiers

Catalog Number
94006 FDA UDI
Primary DI / UDI-DI
05060488572470 FDA UDI
FDA Product Code
FNM FDA UDI
GMDN Term
Alternating-pressure bed mattress overlay system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5550 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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 80 Inch FDA UDI
Width — 60 Inch FDA UDI
Height — 7 Inch FDA UDI

Category: Alternating-pressure bed mattress overlay system

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

Similar devices

Also classified as Alternating-pressure bed mattress overlay system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Proactive Medical Products

Sources (1)

  • FDA UDI f6b744cb-41e8-4894-b895-3aadec3720dc 36 fields · synced Jun 1, 2026