Dansons

FDA UDI

Class I (US FDA UDI)

by Bestcare, L.l.c.

Identity

Trade Name: Dansons FDA UDI
Generic Name: Mobile patient lifting system, manual FDA UDI
Device Name: Dansons PL350H, 350 lb, Manual, Purple and White FDA UDI
Model / Reference: 01 FDA UDI
Description: Dansons PL350H, 350 lb, Manual, Purple and White FDA UDI

Identifiers

Primary DI / UDI-DI: B900DMPL350H010 FDA UDI
FDA Product Code: FMR FDA UDI
GMDN Term: Mobile patient lifting system, manual FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.6785 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Mobile patient lifting system, manual

Dansons by Bestcare, L.l.c. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Bestcare, L.l.c.

Sources (1)

FDA UDI e304da3f-d9cc-4d70-8ba6-bb3f7e6441ca 34 fields · synced May 30, 2026