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Voss Laminectomy Harness

FDA UDI

Class I (US FDA UDI)

by Vm/Positioning, Inc.

Identity

Trade Name
Voss Laminectomy Harness FDA UDI
Generic Name
Arm procedure positioner, reusable FDA UDI
Device Name
Disposable Foam Laminectmy Harness 3" x 5" x 24" FDA UDI
Model / Reference
714-LAC FDA UDI
Description
Disposable Foam Laminectmy Harness 3" x 5" x 24" FDA UDI

Identifiers

Primary DI / UDI-DI
00811304020553 FDA UDI
FDA Product Code
BTX FDA UDI
GMDN Term
Arm procedure positioner, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.3910 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 — 24 Inch FDA UDI

Category: Arm procedure positioner, reusable

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

Similar devices

Also classified as Arm procedure positioner, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7bde7447-f4de-4458-8542-f5a3a65bdbd6 34 fields · synced May 30, 2026