← Back to catalogue

Lifting pole

FDA UDI

Class II (US FDA UDI)

by Paramount Bed Co., Ltd.

Identity

Trade Name
Lifting pole FDA UDI
Generic Name
Assistive patient lifting pole FDA UDI
Device Name
Pole to assist the patient to raise the body from Hospital Bed. FDA UDI
Model / Reference
KA-H70LU FDA UDI
Description
Pole to assist the patient to raise the body from Hospital Bed. FDA UDI

Identifiers

Primary DI / UDI-DI
04527799700271 FDA UDI
FDA Product Code
FNL 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Assistive patient lifting pole

Lifting pole by Paramount Bed Co., Ltd. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 722a5eb6-3778-460f-915b-13b364c43015 33 fields · synced May 30, 2026