← Back to catalogue

Blue Diamond

FDA UDI

Class I (US FDA UDI)

by David Scott Company.

Identity

Trade Name
Blue Diamond FDA UDI
Generic Name
Leg procedure positioner FDA UDI
Device Name
Leg Prepper Support FDA UDI
Model / Reference
DSC-SLPS FDA UDI
Description
Leg Prepper Support FDA UDI

Identifiers

Catalog Number
DSC-SLPS FDA UDI
Primary DI / UDI-DI
15060797552962 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Leg procedure positioner 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

Dimensions & Sizes

Size
Width — 6 Inch FDA UDI
Length — 13 Inch FDA UDI
Height — 33 Inch FDA UDI

Category: Leg procedure positioner

Blue Diamond by David Scott Company. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Leg procedure positioner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1810c111-d233-4b4e-b120-d2d9304df05f 36 fields · synced May 30, 2026