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Protekt

FDA UDI

Class I (US FDA UDI)

by Proactive Medical Products

Identity

Trade Name
Protekt FDA UDI
Generic Name
Handgrip disability-assistive walker, non-powered, non-foldable FDA UDI
Device Name
Protekt Rollator, Steel (PU Seat) Standard, Red, Knock Down FDA UDI
Model / Reference
RLADST6-RD-KD FDA UDI
Description
Protekt Rollator, Steel (PU Seat) Standard, Red, Knock Down FDA UDI

Identifiers

Catalog Number
RLADST6-RD-KD FDA UDI
Primary DI / UDI-DI
05060488573972 FDA UDI
FDA Product Code
IOR FDA UDI
GMDN Term
Handgrip disability-assistive walker, non-powered, non-foldable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3850 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 13 Inch FDA UDI
Height — 37 Inch FDA UDI
Length — 33 Inch FDA UDI

Category: Handgrip disability-assistive walker, non-powered, non-foldable

Protekt by Proactive Medical Products — 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

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Manufacturer

Manufacturer
Proactive Medical Products

Sources (1)

  • FDA UDI d91b6e21-fc64-4990-98d5-b1f90325afb3 36 fields · synced May 30, 2026