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David Scott Company

FDA UDI

Class I (US FDA UDI)

by David Scott Company.

Identity

Trade Name
David Scott Company FDA UDI
Generic Name
Arm procedure positioner, reusable FDA UDI
Device Name
Carbon Fiber Anesthesia Armboard FDA UDI
Model / Reference
DSC-1009-001 FDA UDI
Description
Carbon Fiber Anesthesia Armboard FDA UDI

Identifiers

Catalog Number
DSC-1009-001 FDA UDI
Primary DI / UDI-DI
15060797554188 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Arm procedure positioner, reusable 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

No

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

No

FDA UDI

Category: Arm procedure positioner, reusable

David Scott Company by David Scott Company. — 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 36499319-14c9-4f02-b632-58dea8a08007 35 fields · synced May 30, 2026