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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
Overbed table FDA UDI
Device Name
HOSPICE COMPOSITE TOP OBT GREY, LOCKING KNOB, 25LB CAP FDA UDI
Model / Reference
PB3037C FDA UDI
Description
HOSPICE COMPOSITE TOP OBT GREY, LOCKING KNOB, 25LB CAP FDA UDI

Identifiers

Primary DI / UDI-DI
00815067013395 FDA UDI
FDA Product Code
KMN FDA UDI
INW FDA UDI
GMDN Term
Overbed table FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6140 FDA UDI
890.3750 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: Overbed table

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

Similar devices

Also classified as Overbed table.

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 242914ac-bb42-4172-b0c7-abd951406fa2 34 fields · synced Jun 8, 2026