AccessGUDID - DEVICE: BD Pyxis (10885403510427)

GUDID

Device Identifier (DI) Information

Brand Name: BD Pyxis
Version or Model: iMX105
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: CAREFUSION 303, INC.

Primary DI Number: 10885403510427
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 360624720 *Terms of Use

Device Description: BD Pyxis ES Refrigerator (5 cu ft)

Device Characteristics

What MRI safety information does the labeling contain?	MR Unsafe
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
34885	Anaesthesia cabinet	A furniture-like device, typically designed as a small cupboard on wheels, used for the secure storage of anaesthetic equipment and drugs. It typically includes an appropriate working surface for anaesthetics, instruments, vials, or other small devices. It is usually constructed to prevent the build-up of static electrical charges.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
BRY	CABINET, TABLE AND TRAY, ANESTHESIA

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 6ef2d8a6-4284-48f5-a5e8-2f1bc25d20a5
Public Version Date: August 14, 2023
Public Version Number: 2
DI Record Publish Date: December 02, 2022

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: No
Serial Number: Yes
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(800)727-6102
Email: productcomplaints@bd.com

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