CREATININE PAP SL

GUDID 03661540214301

ELITECH CLINICAL SYSTEMS SAS

Creatinine IVD, kit, enzyme spectrophotometry
Primary Device ID03661540214301
NIH Device Record Keyf414fa6e-cd60-4e77-9de6-0e7eb482a2e8
Commercial Distribution StatusIn Commercial Distribution
Brand NameCREATININE PAP SL
Version Model NumberCRSL-0250
Company DUNS267732378
Company NameELITECH CLINICAL SYSTEMS SAS
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS103661540214301 [Primary]

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2024-09-16
Device Publish Date2016-09-24

Devices Manufactured by ELITECH CLINICAL SYSTEMS SAS

03661540200809 - ENVOY 500 ALT REAGENT KIT2024-09-16
03661540201905 - ENVOY 500 CREATININE REAGENT KIT2024-09-16
03661540202506 - ENVOY 500 ISE BASELINE SOLUTION KIT2024-09-16
03661540202605 - ENVOY 500 ISE CALIBRATOR KIT2024-09-16
03661540202803 - ENVOY 500 ISE REFERENCE SOLUTION KIT2024-09-16
03661540202902 - ENVOY 500 LDL CALIBRATOR KIT2024-09-16
03661540203602 - ENVOY 500 TOTAL PROTEIN REAGENT KIT2024-09-16
03661540203800 - ENVOY 500 BUN REAGENT KIT2024-09-16

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.