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Blue Diamond

FDA UDI

Class I (US FDA UDI)

by David Scott Company.

Identity

Trade Name
Blue Diamond FDA UDI
Generic Name
Operating table patient pressure distribution pad, reusable FDA UDI
Device Name
Reusable Laminectomy Pad FDA UDI
Model / Reference
BD-RLP FDA UDI
Description
Reusable Laminectomy Pad FDA UDI

Identifiers

Catalog Number
BD-RLP FDA UDI
Primary DI / UDI-DI
15060797552764 FDA UDI
FDA Product Code
LWG FDA UDI
GMDN Term
Operating table patient pressure distribution pad, 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

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 — 5 Inch FDA UDI
Length — 5 Inch FDA UDI
Outer Diameter — 2.5 Inch FDA UDI

Category: Operating table patient pressure distribution pad, reusable

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

Similar devices

Also classified as Operating table patient pressure distribution pad, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
David Scott Company.

Sources (1)

  • FDA UDI 7331160f-7397-414e-b697-b9e616d1db5c 36 fields · synced May 30, 2026