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Active Heel Traction Boot

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Active Heel Traction Boot FDA UDI
Generic Name
Heel stirrup cushion/pad, reusable FDA UDI
Device Name
ACTIVE HEEL TRACTION BOOT REPLACEMENT KIT -TOE STRAP FDA UDI
Model / Reference
72203345 FDA UDI
Description
ACTIVE HEEL TRACTION BOOT REPLACEMENT KIT -TOE STRAP FDA UDI

Identifiers

Catalog Number
72203345 FDA UDI
Primary DI / UDI-DI
00885554024845 FDA UDI
FDA Product Code
HST FDA UDI
GMDN Term
Heel stirrup cushion/pad, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.5850 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Heel stirrup cushion/pad, reusable

Active Heel Traction Boot by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Heel stirrup cushion/pad, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI d8d08e8c-f71a-4f3e-a02d-e1bedad45f7c 35 fields · synced Jun 8, 2026