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Banana

FDA UDI

Class II (US FDA UDI)

by Gbuk Ltd

Identity

Trade Name
Banana FDA UDI
Generic Name
Patient lifting system stretcher FDA UDI
Device Name
Banana, Air Assisted Device, Flojac, Reusable, 39" Wide (99cm) FDA UDI
Model / Reference
LUS-FLOJAC-39 FDA UDI
Description
Banana, Air Assisted Device, Flojac, Reusable, 39" Wide (99cm) FDA UDI

Identifiers

Catalog Number
LUS-FLOJAC-39 FDA UDI
Primary DI / UDI-DI
05060405747837 FDA UDI
FDA Product Code
FNG FDA UDI
GMDN Term
Patient lifting system stretcher FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5500 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient lifting system stretcher

Banana by Gbuk Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient lifting system stretcher.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gbuk Ltd

Sources (1)

  • FDA UDI 99e8c881-b386-4015-912d-67f3bade27cc 34 fields · synced May 30, 2026