Primary Device ID | 26970401813210 |
NIH Device Record Key | 2ac10225-b5a7-412f-8897-d360c8451a21 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Rotatable Snares |
Version Model Number | MD-E-SNR243224 |
Company DUNS | 544434963 |
Company Name | Zhe Jiang ChuangXiang Medical Technology 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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06970401811137 [Primary] |
GS1 | 16970401813206 [Package] Contains: 06970401811137 Package: Box [10 Units] In Commercial Distribution |
GS1 | 26970401813210 [Package] Contains: 16970401813206 Package: Case [5 Units] In Commercial Distribution |
FDI | Snare, Flexible |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-02-21 |
Device Publish Date | 2018-09-25 |
26970401813210 | MD-E-SNR243224 |
06970401811120 | MD-E-SNR242524 |
26970401814309 | MD-E-SNR241524 |