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Foot and Ankle Step

FDA UDI

Class I (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
Foot and Ankle Step FDA UDI
Generic Name
Assistive stool/step FDA UDI
Device Name
FOOT AND ANKLE STEP FDA UDI
Model / Reference
Foot and Ankle Step FDA UDI
Description
FOOT AND ANKLE STEP FDA UDI

Identifiers

Catalog Number
1743616 FDA UDI
Primary DI / UDI-DI
60889971743619 FDA UDI
FDA Product Code
FZM FDA UDI
GMDN Term
Assistive stool/step 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Assistive stool/step

Foot and Ankle Step by Carestream Health, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assistive stool/step.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0487867a-84d9-49a8-94a1-3cd3a31f4a80 34 fields · synced Jun 8, 2026