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MediChoice

FDA UDI

Class I (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
MediChoice FDA UDI
Generic Name
Nurse call system alarm FDA UDI
Device Name
Patient Safety Alarm Nurse Call Cable Y-splitter Not Made With Natural Rubber Latex Reusable MediChoice FDA UDI
Model / Reference
PSNCY1 FDA UDI
Description
Patient Safety Alarm Nurse Call Cable Y-splitter Not Made With Natural Rubber Latex Reusable MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632066979 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Nurse call system alarm FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2400 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nurse call system alarm

MediChoice by Owens & Minor Distribution, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nurse call system alarm.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI aa0d062a-9c6a-4cd6-b350-73c2c8011f9c 33 fields · synced May 31, 2026