Primary Device ID | 06925912716785 |
NIH Device Record Key | 56770aa3-1ec0-47f9-a16a-bb76a9933b8f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sample Diluent |
Version Model Number | C89919-1 |
Company DUNS | 420735989 |
Company Name | Shenzhen YHLO Biotech Co., Ltd. |
Device Count | 100 |
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 | false |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06925912716785 [Unit of Use] |
GS1 | 06925912716792 [Primary] |
PPM | General Purpose Reagent |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-03 |
Device Publish Date | 2022-10-26 |
06925912716785 | Sample Diluent I-1, 0.57 mL×100 PCS |
06925912716709 | Sample Diluent I, 45 mL×2 bottles |
06925912716686 | Sample Diluent H, 45 mL×2 bottles |
06925912716655 | Sample Diluent G, 45 mL×2 bottles |
06925912716662 | Sample Diluent D, 45 mL×2 bottles |
06925912716778 | Sample Diluent D, 120 microliter x100 PCS |
06925912716617 | Sample Diluent B, 45 mL×2 bottles |
06925912716594 | Sample Diluent A, 45 mL×2 bottles |