← Back to catalogue

Imperial Stackable Stepstool

FDA UDI

Class I (US FDA UDI)

by Imperial Surgical Ltd

Identity

Trade Name
Imperial Stackable Stepstool FDA UDI
Generic Name
Footstool FDA UDI
Device Name
Footstool With HR\16Lx12Wx8H FDA UDI
Model / Reference
OR-36360-H FDA UDI
Description
Footstool With HR\16Lx12Wx8H FDA UDI

Identifiers

Catalog Number
OR-36360-H FDA UDI
Primary DI / UDI-DI
07540162040412 FDA UDI
FDA Product Code
FZM FDA UDI
GMDN Term
Footstool 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Footstool

Imperial Stackable Stepstool by Imperial Surgical Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Footstool.

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 12e2be54-983e-4b1f-b35d-7a327650f7f2 35 fields · synced Jun 8, 2026