| Primary Device ID | 26952534441027 |
| NIH Device Record Key | 5cbfc4b4-dab0-4d9d-a49b-83b679adb5f9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Senolo |
| Version Model Number | XP2 |
| Company DUNS | 421315790 |
| Company Name | JIANGSU SENOLO MEDICAL TECHNOLOGY CO., LTD. |
| Device Count | 1 |
| 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 | 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 | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 26952534441027 [Primary] |
| ITG | Bandage, Cast |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-04-14 |
| Device Publish Date | 2023-04-06 |
| 26952534451040 | XE43 |
| 26952534451033 | XE33 |
| 26952534451026 | XE23 |
| 26952534441089 | XP8 |
| 26952534441065 | XP6 |
| 26952534441041 | XP4 |
| 26952534441034 | XP3 |
| 26952534441027 | XP2 |
| 26952534431035 | 5l |
| 26952534431028 | 1l |
| 26952534431011 | 250ml |
| 16952534421169 | XB546 |
| 16952534421152 | XB530 |
| 16952534421145 | XB430 |
| 16952534421138 | XB416 |
| 16952534421121 | XB336 |
| 16952534421114 | XB312 |
| 16952534421060 | XB6 |
| 16952534421053 | XB5 |
| 16952534421046 | XB4 |
| 16952534421039 | XB3 |
| 16952534421022 | XB2 |
| 16952534411160 | XD6 |
| 16952534411153 | XD5 |
| 16952534411146 | XD4 |
| 16952534411139 | XD3 |
| 16952534411122 | XD2 |