| Primary Device ID | 90850010779303 |
| NIH Device Record Key | 58ed1ace-0715-4071-b9a1-667d4885ce58 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Robbins Microcannulas |
| Version Model Number | 21.CAN-FIC2250 |
| Catalog Number | 21.CAN-FIC2250 |
| Company DUNS | 002182269 |
| Company Name | Robbins Instruments Inc |
| Device Count | 20 |
| 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 | true |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | +1(973)635-8972 |
| info@robbinsinstruments.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10850010779307 [Unit of Use] |
| GS1 | 90850010779303 [Primary] |
| FGY | CANNULA, INJECTION |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[90850010779303]
Ethylene Oxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2020-02-27 |
| Device Publish Date | 2019-10-25 |
| 98500107790323 | Robbins Microcannulas 27Gx40mm |
| 98500107790316 | Robbins Microcannulas 25Gx50mm |
| 98500107790309 | Robbins Microcannulas 22Gx50mm |
| 90850010779327 | Robbins Microcannulas 27Gx40mm |
| 90850010779310 | Robbins Microcannulas 25Gx50mm |
| 90850010779303 | Robbins Microcannulas 22Gx50mm |