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Protekt Parts

FDA UDI

Class I (US FDA UDI)

by Proactive Medical Products

Identity

Trade Name
Protekt Parts FDA UDI
Generic Name
Wheelchair/chair/stander occupant restraint/support FDA UDI
Device Name
Universal Reat Anti-Tipper w/ Wheels (STDS807) FDA UDI
Model / Reference
PP-RATWW FDA UDI
Description
Universal Reat Anti-Tipper w/ Wheels (STDS807) FDA UDI

Identifiers

Catalog Number
PP-RATWW FDA UDI
Primary DI / UDI-DI
05060488573019 FDA UDI
FDA Product Code
IML FDA UDI
GMDN Term
Wheelchair/chair/stander occupant restraint/support FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3920 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

Dimensions & Sizes

Size
Height — 4 Inch FDA UDI
Length — 8 Inch FDA UDI
Width — 2 Inch FDA UDI

Category: Wheelchair/chair/stander occupant restraint/support

Protekt Parts by Proactive Medical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair/chair/stander occupant restraint/support.

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 d79a8351-1275-437c-8a5d-0f8acb741df8 36 fields · synced May 31, 2026