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ProBasics

FDA UDI

Class II (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
ProBasics FDA UDI
Generic Name
Bedrail FDA UDI
Device Name
Half Length Bed Rails FDA UDI
Model / Reference
PB7035 FDA UDI
Description
Half Length Bed Rails FDA UDI

Identifiers

Catalog Number
PB7035 FDA UDI
Primary DI / UDI-DI
00815067071302 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Bedrail 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

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

Yes

FDA UDI

Category: Bedrail

ProBasics by Compass Health Brands Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bedrail.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 570d4f27-a71a-4c23-9e90-7fa4bafdce96 35 fields · synced May 30, 2026