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BestStand

FDA UDI

Class I (US FDA UDI)

by Bestcare, L.l.c.

Identity

Trade Name
BestStand FDA UDI
Generic Name
Mobile patient lifting system, manual FDA UDI
Device Name
Bestcare BestStand SA182H, 400lb, Manual, U-Shaped 4pt Boom, Red and White, GS FDA UDI
Model / Reference
01 FDA UDI
Description
Bestcare BestStand SA182H, 400lb, Manual, U-Shaped 4pt Boom, Red and White, GS FDA UDI

Identifiers

Primary DI / UDI-DI
B900SA182H010 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

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: Mobile patient lifting system, manual

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

Similar devices

Also classified as Mobile patient lifting system, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bestcare, L.l.c.

Sources (1)

  • FDA UDI 2b1b7fba-1443-4f03-908d-4b7d1232760c 34 fields · synced May 30, 2026