C-KUP Liquefaction Test Cup

GUDID 44719874740724

BONRAYBIO CO., LTD.

General specimen container IVD, no additive
Primary Device ID44719874740724
NIH Device Record Key26181d0b-6f1e-47d6-af25-a1dc4689a8f2
Commercial Distribution StatusIn Commercial Distribution
Brand NameC-KUP Liquefaction Test Cup
Version Model NumberCK0_200pcs
Company DUNS658872369
Company NameBONRAYBIO CO., LTD.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS144719874740724 [Primary]

FDA Product Code

NNIContainer, Specimen, Non-Sterile

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-07-19
Device Publish Date2021-07-09

On-Brand Devices [C-KUP Liquefaction Test Cup]

14719874740723CK0
44719874740779CK0_200pcs-BR USA CORP.
44719874740724CK0_200pcs

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.