| Primary Device ID | 08903347002367 |
| NIH Device Record Key | 5ed13c5b-4516-43bc-91c3-463034fe6fc0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UNOLOK+ |
| Version Model Number | 25G X ¾" |
| Catalog Number | 00236 |
| Company DUNS | 862318107 |
| Company Name | HINDUSTAN SYRINGES AND MEDICAL DEVICES LIMITED |
| 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 | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08903347002367 [Primary] |
| GS1 | 18903347002364 [Package] Package: BOX [100 Units] In Commercial Distribution |
| GS1 | 28903347002361 [Package] Contains: 18903347002364 Package: CARTON [10 Units] In Commercial Distribution |
| GS1 | 58903347002362 [Package] Contains: 28903347002361 Package: PALLET [14 Units] In Commercial Distribution |
| FPA | Set, Administration, Intravascular |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-10-23 |
| Device Publish Date | 2017-04-26 |
| 08903347002367 | UNOLOK+ Luer Lock Infusion Set,25 G X ¾" ( 0.50X19MM) 7" TUBE MYCO RE-ORDER # 7001P-25L |
| 08903347002350 | UNOLOK+ Luer Lock Infusion Set,23 G X ¾" ( 0.60X19MM) 7" TUBE MYCO RE-ORDER # 7001P-23L |
| 08903347002343 | UNOLOK+ Luer Lock Infusion Set,21 G X ¾" ( 0.80X19MM) 7" TUBE MYCO RE-ORDER # 7001P-21L |
| 08903347002336 | UNOLOK+ Luer Lock Infusion Set,19 G X ¾" ( 1.10X19MM) 7" TUBE MYCO RE-ORDER # 7001P-19L |