| Primary Device ID | 50886333622424 |
| NIH Device Record Key | dcbeec7b-ef34-4b02-b666-7c0900c278b4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SY12-RTR |
| Version Model Number | 682242 |
| Catalog Number | 682242 |
| Company DUNS | 595138793 |
| Company Name | ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. |
| 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 | true |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | 1.800.927.4669 |
| Customer.Service@argonmedical.com | |
| Phone | 1.800.927.4669 |
| Customer.Service@argonmedical.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00886333622429 [Primary] |
| GS1 | 50886333622424 [Package] Contains: 00886333622429 Package: Tyvek Bag [50 Units] In Commercial Distribution |
| DQF | Actuator, Syringe, Injector Type |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-30 |
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