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RadBoard®Xtra™

FDA UDI

Class I (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
RadBoard®Xtra™ FDA UDI
Generic Name
Arm procedure positioner, reusable FDA UDI
Model / Reference
00884450203200 FDA UDI

Identifiers

Primary DI / UDI-DI
00884450203200 FDA UDI
FDA Product Code
BWN FDA UDI
GMDN Term
Arm procedure positioner, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Arm procedure positioner, reusable

Radiate arm positioning and stabilization with the RadBoard Xtra, a preformed device designed for use in various medical procedures. This reusable device provides adjustable height, tilt, rotation, and lock positioning capabilities, allowing healthcare professionals to safely and effectively position patients.

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

Manufacturer
Merit Medical Systems, Inc.

Sources (1)

  • FDA UDI 83aca0c6-f6a2-4031-9bc7-1bdeccaa29f2 32 fields · synced Jul 25, 2026