| Primary Device ID | 00761059015017 |
| NIH Device Record Key | 352a613d-5790-43b7-880f-60226b818a57 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Universal Sharps Container |
| Version Model Number | SC0015 |
| Company DUNS | 968012943 |
| Company Name | POST MEDICAL, INC. |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00761059015017 [Primary] |
| FMI | Needle, Hypodermic, Single Lumen |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-02-28 |
| Device Publish Date | 2022-02-20 |
| 00761059015017 - Universal Sharps Container | 2022-02-28 |
| 00761059015017 - Universal Sharps Container | 2022-02-28 |
| B3091101LPBW0 - Post Medical, Inc. | 2018-07-06 |
| B3091101LPR0 - Post Medical, Inc. | 2018-07-06 |
| B3091G1 - Post Medical, Inc. | 2018-07-06 |
| B3092201LPBW1 - Post Medical, Inc. | 2018-07-06 |
| B3092201LPBWY1 - Post Medical, Inc. | 2018-07-06 |
| B3092201LPR1 - Post Medical, Inc. | 2018-07-06 |
| B3092G1 - Post Medical, Inc. | 2018-07-06 |