Inoculating Loop Typenex LP0103

GUDID 16973267011038

1ul, Flexible, Blue

ZHEJIANG RUNLAB TECHNOLOGY CO., LTD

Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD Specimen transfer scooping tool IVD
Primary Device ID16973267011038
NIH Device Record Key6b487137-d417-45ac-9a1d-cb3fce5f791e
Commercial Distribution StatusIn Commercial Distribution
Brand NameInoculating Loop Typenex
Version Model Number1ul, Flexible, Blue
Catalog NumberLP0103
Company DUNS529124298
Company NameZHEJIANG RUNLAB TECHNOLOGY 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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS106973267011031 [Primary]
GS106973267011055 [Package]
Contains: 06973267011031
Package: inner bag [50 Units]
In Commercial Distribution
GS116973267011038 [Package]
Contains: 06973267011031
Package: case [6 Units]
In Commercial Distribution

FDA Product Code

LIBDevice, General Purpose, Microbiology, Diagnostic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-04
Device Publish Date2023-07-27

On-Brand Devices [Inoculating Loop Typenex]

1697326701203510ul, Flexible, Blue
1697326701202810ul, Rigid, Dark blue
169732670110381ul, Flexible, Blue
169732670110211ul, Rigid, Dark blue

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