← Back to catalogue

Stackable Foot Stool without mat

FDA UDI

Class I (US FDA UDI)

by Batrik Medical Manufacturing Inc

Identity

Trade Name
Stackable Foot Stool without mat FDA UDI
Generic Name
Footstool FDA UDI
Device Name
Stackable Steptool without mat, Autoclavable FDA UDI
Model / Reference
OR-36364 FDA UDI
Description
Stackable Steptool without mat, Autoclavable FDA UDI

Identifiers

Catalog Number
OR-36364 FDA UDI
Primary DI / UDI-DI
00690521013964 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Footstool

Stackable Foot Stool without mat by Batrik Medical Manufacturing Inc — 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 827d8760-896b-49f3-a8ef-4021dcbb2e0a 36 fields · synced May 29, 2026