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 |