AccessGUDID - DEVICE: Temperature Probes (00884838006942)

GUDID

Device Identifier (DI) Information

Brand Name: Temperature Probes
Version or Model: Ice Bath Temperature Probe
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 23002A
Company Name: Philips Medical Systems Hsg

Primary DI Number: 00884838006942
Issuing Agency: GS1
Commercial Distribution End Date: November 01, 2024
Device Count: 1
Labeler D-U-N-S® Number*: 790605856 *Terms of Use

Device Description: Ice Bath Temperature Probe Reusable static temperature probe to measure cardiac output using an ice bath and syringes; Length(including probe) = 10' (3m); Wgt = 3 oz (85g)

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?
37340	General-purpose patient temperature probe, reusable	A temperature sensing device intended to be placed into a body orifice or on the body surface and used in conjunction with a separate parent device with a display (e.g., electronic patient thermometer, infant warmer) to enable measurement/monitoring of a patient’s temperature; its use is not dedicated to a specific type of procedure. It is typically constructed of flexible materials (e.g., plastic or rubber) with a metal conducting core; the distal end of different device types will be designed for a particular application site. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MHX	MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)

FDA Premarket Submission

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

Device Exempt from Premarket Submission: No 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
Storage Environment Temperature: between -40 and 50 Degrees Celsius
Storage Environment Temperature: between -40 and 122 Degrees Fahrenheit

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: ea0e8dfb-a5eb-4496-9790-625bedb682d7
Public Version Date: November 26, 2024
Public Version Number: 8
DI Record Publish Date: June 09, 2017