| Primary Device ID | 06925912716617 | 
| NIH Device Record Key | 04eec195-7055-481b-831e-e37b82b72e2b | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Sample Diluent | 
| Version Model Number | C89912 | 
| Company DUNS | 420735989 | 
| Company Name | Shenzhen YHLO Biotech Co., Ltd. | 
| Device Count | 2 | 
| 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 | 06925912716600 [Primary] | 
| GS1 | 06925912716617 [Unit of Use] | 
| 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 |