Primary Device ID | 06973267011161 |
NIH Device Record Key | eb9ca7a0-ea59-46f7-bf97-f2fb3e2656e3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Inoculating Loop 1ul Typenex |
Version Model Number | 1ul,rigid,dark blue, LP0102 |
Catalog Number | LP0102 |
Company DUNS | 529124298 |
Company Name | ZHEJIANG RUNLAB TECHNOLOGY CO., LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06973267011123 [Package] Contains: 06973267011147 Package: inner box [50 Units] In Commercial Distribution |
GS1 | 06973267011147 [Package] Package: inner bag [20 Units] In Commercial Distribution |
GS1 | 06973267011161 [Primary] |
GS1 | 16973267011120 [Package] Contains: 06973267011123 Package: case [6 Units] In Commercial Distribution |
LIB | Device, General Purpose, Microbiology, Diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-10-18 |
Device Publish Date | 2023-10-10 |
06973267011154 | 1ul,flexible, blue, LP0103 |
06973267011161 | 1ul,rigid,dark blue, LP0102 |