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Autologic

FDA UDI

Class II (US FDA UDI)

by Arjohuntleigh, Inc.

Identity

Trade Name
AUTOLOGIC FDA UDI
Generic Name
Alternating-pressure bed mattress overlay system FDA UDI
Device Name
Mattress - Alternating Pressure - Auto Logic 175 (Reliant IS) Length 2030mm (80"), Width 860mm (34"), Height 175mm (7") FDA UDI
Model / Reference
PXB005DAR FDA UDI
Description
Mattress - Alternating Pressure - Auto Logic 175 (Reliant IS) Length 2030mm (80"), Width 860mm (34"), Height 175mm (7") FDA UDI

Identifiers

Primary DI / UDI-DI
05055982782395 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

Yes

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: Alternating-pressure bed mattress overlay system

Autologic by Arjohuntleigh, Inc. — 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
Arjohuntleigh, Inc.

Sources (1)

  • FDA UDI 9fe8def3-7a9f-41a1-9d36-757fa9f74897 33 fields · synced May 31, 2026