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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
Leg procedure positioner FDA UDI
Device Name
Replacement stirrup boot liners for Allen ®Pal Style Stirrups. Made of a doughy soft visco-memory foam, the wide front flaps Velcro secure and hold leg in place. Reusable and easily cleaned FDA UDI
Model / Reference
BD-AFHBP FDA UDI
Description
Replacement stirrup boot liners for Allen ®Pal Style Stirrups. Made of a doughy soft visco-memory foam, the wide front flaps Velcro secure and hold leg in place. Reusable and easily cleaned FDA UDI

Identifiers

Catalog Number
BD-AFHBP FDA UDI
Primary DI / UDI-DI
15060797552382 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 — 26 Inch FDA UDI
Length — 41 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

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Manufacturer

Sources (1)

  • FDA UDI 56cee2d5-fc47-47a9-bb24-c4310897f563 36 fields · synced Jun 8, 2026