| Primary Device ID | 08903347023423 |
| NIH Device Record Key | 042e066f-0cdf-43d9-8faa-b92781602f13 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VAKU-8+ |
| Version Model Number | 21 G X ¾" |
| Catalog Number | 02342 |
| 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 | 08903347023423 [Primary] |
| GS1 | 18903347023420 [Package] Package: BOX [100 Units] In Commercial Distribution |
| GS1 | 28903347023427 [Package] Contains: 18903347023420 Package: CARTON [10 Units] In Commercial Distribution |
| GS1 | 58903347023428 [Package] Contains: 28903347023427 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 |
| 08903347023447 | VAKU-8 + Blood Collection Set,25 G X ¾" ( 0.50X19MM) 7" TUBE MYCO RE-ORDER # SVMSP-25L |
| 08903347023430 | VAKU-8+ Blood Collection Set,23 G X ¾" ( 0.60X19MM) 7" TUBE MYCO RE-ORDER # SVMSP-23L |
| 08903347023423 | VAKU-8 + Blood Collection Set,21 G X ¾" ( 0.80X19MM) 7" TUBE MYCO RE-ORDER # SVMSP-21L |