AccessGUDID - DEVICE: Bio-Probe® (00673978563336)

GUDID

Device Identifier (DI) Information

Brand Name: Bio-Probe®
Version or Model: CB4627
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: MEDTRONIC, INC.

Primary DI Number: 00673978563336
Issuing Agency: GS1
Commercial Distribution End Date: November 30, 2017
Device Count: 1
Labeler D-U-N-S® Number*: 006261481 *Terms of Use

Device Description: CONN PROBE CB4627 BIOACT FLOW PEDIATRIC

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):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	Yes
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?
31657	Blood flowmeter transducer, non-indwelling	A device designed to be used together with a blood flowmeter for the continuous external (extravascular) measurement of a patient's blood flow. It may measure the blood flow either in a closed chamber that encompasses the transducer outside of the body or over the outside of a blood vessel (formed as an open circle which is slid over the vessel, having different diameters to fit different size blood vessels). It may function by using ultrasound or electromagnetic (EM) technologies. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DPT	PROBE, BLOOD-FLOW, EXTRAVASCULAR

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K830858	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

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

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: less than 40 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: ddebdaf5-01a6-4f3b-bac6-7277f831f206
Public Version Date: July 06, 2018
Public Version Number: 3
DI Record Publish Date: June 16, 2016

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
20673978563330	10	00673978563336	2017-11-30	Not in Commercial Distribution	PK

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: Yes
Serial Number: No
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(800)633-8766
Email: Corporate.UDI@medtronic.com

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