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Pyxis Pro MedStation

FDA UDI

Class I (US FDA UDI)

by CareFusion 303, INC

Identity

Trade Name
Pyxis Pro MedStation FDA UDI
Generic Name
Anaesthesia cabinet FDA UDI
Device Name
Pyxis Pro MedStation Dispensing System cabinet, table and tray, anesthesia FDA UDI
Model / Reference
177-142 FDA UDI
Description
Pyxis Pro MedStation Dispensing System cabinet, table and tray, anesthesia FDA UDI

Identifiers

Catalog Number
177-142 FDA UDI
Primary DI / UDI-DI
10885403528057 FDA UDI
FDA Product Code
BRY FDA UDI
GMDN Term
Anaesthesia cabinet FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6100 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Anaesthesia cabinet

Pyxis Pro MedStation by CareFusion 303, INC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia cabinet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
CareFusion 303, INC

Sources (1)

  • FDA UDI 9cf6e63b-2b97-4bd7-bb44-a1bfb5ec18f1 36 fields · synced May 30, 2026