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Patient Helper

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Patient Helper FDA UDI
Generic Name
Assistive patient lifting pole FDA UDI
Model / Reference
5900 FDA UDI

Identifiers

Catalog Number
5900-000-145 FDA UDI
Primary DI / UDI-DI
07613327419252 FDA UDI
FDA Product Code
OSI FDA UDI
GMDN Term
Assistive patient lifting pole FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5100 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 patient lifting pole

Patient Helper by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assistive patient lifting pole.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 7e6a5346-24f8-4758-8f65-bf3d0b021689 34 fields · synced May 30, 2026