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Body Positioning Wedge

FDA UDI

Class I (US FDA UDI)

by Geneva Healthcare, Llc

Identity

Trade Name
Body Positioning Wedge FDA UDI
Generic Name
Freestanding patient positioner, single-use FDA UDI
Device Name
Body Positioning Wedge 23" X 11" X 11" FDA UDI
Model / Reference
101 FDA UDI
Description
Body Positioning Wedge 23" X 11" X 11" FDA UDI

Identifiers

Catalog Number
101 FDA UDI
Primary DI / UDI-DI
10810044960935 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Freestanding patient positioner, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Freestanding patient positioner, single-use

Body Positioning Wedge by Geneva Healthcare, Llc — 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 4855d372-5d0b-4a86-b71a-3bad418f584d 35 fields · synced May 30, 2026