AccessGUDID - DEVICE: NICaS (07290015331005)

GUDID

Device Identifier (DI) Information

Brand Name: NICaS
Version or Model: CS
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: NEW N.I. MEDICAL (2011) LTD

Primary DI Number: 07290015331005
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 600279405 *Terms of Use

Device Description: Bioimpedance Cardiac Analyzing Measuring System

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:	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?
12103	Impedance cardiograph	A device that records the variations in thoracic electrical impedance caused by the activity of the heart muscle, usually detected at the body surface. A current is passed through the body and the product of this current and the body impedance is the electrical potential difference between two sensing electrodes. The graphic representation of the variation of the impedance with time is recorded in a diagram (impedance cardiogram). It is used to study the action of the heart muscle, for diagnosis of specific cardiac abnormalities, and to reveal trends or changes in heart function, especially cardiac output. Some types may include additional measurements (e.g., pulse oximetry, blood pressure).	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DSB	Plethysmograph, Impedance

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K080941	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: 1cbb66a0-6ea4-4706-b0eb-a6c95cbe0448
Public Version Date: May 05, 2023
Public Version Number: 1
DI Record Publish Date: April 27, 2023

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: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

No Customer Contact currently defined

MENU
- Home
- About
- News
- API
- Download
- Help

FDA TOOLS & RESOURCES