AccessGUDID - DEVICE: Tarry Probes (00854758006117)

GUDID

Device Identifier (DI) Information

Brand Name: Tarry Probes
Version or Model: T 08730P
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: T 08730P
Company Name: TARRY MEDICAL PRODUCTS, INC.

Primary DI Number: 00854758006117
Issuing Agency: GS1
Commercial Distribution End Date: April 14, 2020
Device Count: 1
Labeler D-U-N-S® Number*: 107260002 *Terms of Use

Device Description: T 08730P Single Use Skin Temperature Probe

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
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:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	Yes
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?
35254	General-purpose patient temperature probe, single-use	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 single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FMZ	Incubator, Neonatal
FMT	Warmer, Infant Radiant

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K071977	000

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 5908fd80-64f8-4cd9-ba6d-7e9a7ecb5e78
Public Version Date: May 06, 2025
Public Version Number: 4
DI Record Publish Date: September 20, 2016