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Therakair Visio

FDA UDI

Class II (US FDA UDI)

by Arjohuntleigh, Inc.

Identity

Trade Name
THERAKAIR VISIO FDA UDI
Generic Name
Alternating-pressure bed mattress overlay system FDA UDI
Device Name
Mattress - Alternating Pressure - Therakair Visio - Length 208 cm, Width 80 cm, Height 20cm FDA UDI
Model / Reference
M6265529 FDA UDI
Description
Mattress - Alternating Pressure - Therakair Visio - Length 208 cm, Width 80 cm, Height 20cm FDA UDI

Identifiers

Primary DI / UDI-DI
05055982784146 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
Not 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

Therakair Visio by Arjohuntleigh, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Arjohuntleigh, Inc.

Sources (1)

  • FDA UDI 830c56c2-042b-4bb6-84af-a19a0e6f0e96 34 fields · synced Jun 8, 2026