| Primary Device ID | 16973062320397 |
| NIH Device Record Key | 12fbb544-d9bd-48d0-a4de-cc47e7de70cc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Reinforce Surgical Gown (AAMI Level 3) |
| Version Model Number | PM5015RGS |
| Company DUNS | 529796225 |
| Company Name | Foshan Nanhai Plus Medical Co., 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 | false |
| 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 | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06973062320390 [Primary] |
| GS1 | 16973062320397 [Package] Contains: 06973062320390 Package: [50 Units] In Commercial Distribution |
| FYA | Gown, Surgical |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-10-06 |
| Device Publish Date | 2021-09-28 |
| 16973062320199 | PM5005RGS |
| 16973062320182 | PM5004RGS |
| 16973062320175 | PM5003RGS |
| 16973062320168 | PM5002RGS |
| 16973062320151 | PM5001RGS |
| 06973062320147 | PM5005RGN |
| 06973062320130 | PM5004RGN |
| 06973062320123 | PM5003RGN |
| 06973062320116 | PM5002RGN |
| 06973062320109 | PM5001RGN |
| 16973062320397 | PM5015RGS |
| 16973062320380 | PM5014RGS |
| 16973062320373 | PM5013RGS |
| 16973062320366 | PM5012RGS |
| 16973062320359 | PM5011RGS |
| 06973062320345 | PM5015RGN |
| 06973062320338 | PM5014RGN |
| 06973062320321 | PM5013RGN |
| 06973062320314 | PM5012RGN |
| 06973062320307 | PM5011RGN |