← Back to catalogue

McKesson

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Handgrip disability-assistive walker, non-powered, non-foldable FDA UDI
Device Name
Lightweight Rollator red aluminum frame | with 7.5-inch wheels 33 - 38 in Handle height FDA UDI
Model / Reference
146-R728RD FDA UDI
Description
Lightweight Rollator red aluminum frame | with 7.5-inch wheels 33 - 38 in Handle height FDA UDI

Identifiers

Primary DI / UDI-DI
00612479261709 FDA UDI
FDA Product Code
ITJ FDA UDI
GMDN Term
Handgrip disability-assistive walker, non-powered, non-foldable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3825 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: Handgrip disability-assistive walker, non-powered, non-foldable

McKesson by Mckesson Medical-Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Handgrip disability-assistive walker, non-powered, non-foldable.

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

Manufacturer
Mckesson Medical-Surgical Inc.

Sources (1)

  • FDA UDI ec661d1c-9d45-4900-9043-b60984f2f875 33 fields · synced May 31, 2026