| Primary Device ID | 04942962602983 |
| NIH Device Record Key | dc0f2f5e-c918-43a4-bdb0-9e660d354d99 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Test Bag, 50mL |
| Version Model Number | 60298 |
| Catalog Number | 60298 |
| Company DUNS | 690632047 |
| Company Name | ATOM MEDICAL CORPORATION |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | +81488533661 |
| hitoshi.hayashi@atomed.co.jp |
| Total Volume | 50 Milliliter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04942962602983 [Primary] |
| GS1 | 14942962602980 [Package] Package: box [5 Units] In Commercial Distribution |
| BTL | Ventilator, Emergency, Powered (Resuscitator) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-01-29 |
| Device Publish Date | 2015-10-23 |
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