| Primary Device ID | 00857682008110 |
| NIH Device Record Key | 80a573bf-325b-411b-b570-f7298ba13e98 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BH Supplies |
| Version Model Number | BHI1318 |
| Company DUNS | 038516520 |
| Company Name | Anrel Distribution LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00857682008110 [Primary] |
| FMF | Syringe, Piston |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-08-03 |
| Device Publish Date | 2023-07-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BH SUPPLIES 88759405 not registered Live/Pending |
Anr Trade LLC 2020-01-15 |