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Voss Medium Body Wedge

FDA UDI

Class I (US FDA UDI)

by Vm/Positioning, Inc.

Identity

Trade Name
Voss Medium Body Wedge FDA UDI
Generic Name
Freestanding patient positioner, single-use FDA UDI
Device Name
Disposable foam medium body wedge 8" x 8" x 17" FDA UDI
Model / Reference
714-MBW FDA UDI
Description
Disposable foam medium body wedge 8" x 8" x 17" FDA UDI

Identifiers

Primary DI / UDI-DI
00811304020546 FDA UDI
FDA Product Code
KDD FDA UDI
GMDN Term
Freestanding patient positioner, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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 — 17 Inch FDA UDI

Category: Freestanding patient positioner, single-use

Voss Medium Body Wedge by Vm/Positioning, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding patient positioner, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1849e4e5-a013-4b87-9555-77dee6413a05 34 fields · synced Jun 6, 2026