AccessGUDID - DEVICE: 905-918 ABL90 FLEX flush device (05700699059185)

GUDID

Device Identifier (DI) Information

Brand Name: 905-918 ABL90 FLEX flush device
Version or Model: 905-918
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 905-918
Company Name: Radiometer Medical ApS

Primary DI Number: 05700699059185
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 308667539 *Terms of Use

Device Description: Flush device for ABL90 FLEX

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):	Yes
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?
56667	Metabolic profile clinical chemistry analyser IVD	A portable, electrically-powered automated or semi-automated laboratory instrument intended to be used for the qualitative and/or quantitative in vitro measurement of multiple clinical chemistry analytes to generate a metabolic profile. Analytes may include pH, blood gas parameters (e.g., pO2, pCO2), electrolytes [e.g., Sodium (Na2+), potassium (K+), chloride (Cl-)], glucose, urea, creatinine and sometimes in addition haemoximetry parameters [e.g., carboxy-haemoglobin (COHb), methaemoglobin (MetHb), total haemoglobin (totHb), hematrocrit (Hct)].	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JJY	Multi-analyte controls, all kinds (assayed)
CGA	GLUCOSE OXIDASE, GLUCOSE
JFP	ELECTRODE, ION SPECIFIC, CALCIUM
GKR	SYSTEM, HEMOGLOBIN, AUTOMATED
JIX	Calibrator, multi-analyte mixture
GHS	ASSAY, CARBOXYHEMOGLOBIN
CGZ	ELECTRODE, ION-SPECIFIC, CHLORIDE
MQM	BILIRUBIN (TOTAL AND UNBOUND) IN THE NEONATE TEST SYSTEM
CEM	ELECTRODE, ION SPECIFIC, POTASSIUM
CHL	Electrode measurement, blood-gases (pco2, po2) and blood ph
KQI	ASSAY, FETAL HEMOGLOBIN
JGS	ELECTRODE, ION SPECIFIC, SODIUM
KHP	ACID, LACTIC, ENZYMATIC METHOD

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 5b48aeb9-679a-4505-a311-c974ebecaebc
Public Version Date: July 04, 2024
Public Version Number: 4
DI Record Publish Date: September 21, 2018