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Coulmed

FDA UDI

Class I (US FDA UDI)

by Coulmed Products Group Llc

Identity

Trade Name
Coulmed FDA UDI
Generic Name
Leg procedure positioner FDA UDI
Device Name
Replacement FootHugger Boot Pads for Allen PAL Pro, PAL, and SAM III Surgical Stirrups. FDA UDI
Model / Reference
AC3400-BP FDA UDI
Description
Replacement FootHugger Boot Pads for Allen PAL Pro, PAL, and SAM III Surgical Stirrups. FDA UDI

Identifiers

Catalog Number
AC3400-BP FDA UDI
Primary DI / UDI-DI
10810087352629 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

Yes

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: Leg procedure positioner

Coulmed by Coulmed Products Group Llc — 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 3a38e123-ae83-4c80-b44e-44b36805cde0 34 fields · synced Jun 8, 2026