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Probasics

FDA UDI

Class I (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
PROBASICS FDA UDI
Generic Name
Mobile patient lifting system, manual FDA UDI
Device Name
PROBASICS BARIATRIC TRAPEZE - WT CAP 1,000 LBS (LEGS) FDA UDI
Model / Reference
PBBT002 FDA UDI
Description
PROBASICS BARIATRIC TRAPEZE - WT CAP 1,000 LBS (LEGS) FDA UDI

Identifiers

Primary DI / UDI-DI
00815067077021 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
Mobile patient lifting system, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5510 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

Yes

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: Mobile patient lifting system, manual

Probasics by Compass Health Brands Corp. — 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
Compass Health Brands Corp.

Sources (1)

  • FDA UDI 1097bf92-7cc7-46cf-8df3-47d5d92179a1 34 fields · synced May 29, 2026