← 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
Medical table restraint anchor FDA UDI
Device Name
Nylon Restraint Strap with Gel Mid Panel FDA UDI
Model / Reference
BD500-G FDA UDI
Description
Nylon Restraint Strap with Gel Mid Panel FDA UDI

Identifiers

Catalog Number
BD500-G FDA UDI
Primary DI / UDI-DI
15060797554171 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Medical table restraint anchor 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: Medical table restraint anchor

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

Similar devices

Also classified as Medical table restraint anchor.

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 e0870faa-0747-4b80-b6de-bd0b3652bb7d 35 fields · synced Jun 6, 2026