Primary Device ID | 06924274953982 |
NIH Device Record Key | ab191f66-7bc0-43f9-a28e-de033e28f01e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Disposable Electrode Serie |
Version Model Number | OB-2008 |
Company DUNS | 421340711 |
Company Name | Zhejiang Shuyou Surgical Instrument 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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06924274953951 [Primary] |
GS1 | 06924274953968 [Package] Contains: 06924274953951 Package: [5 Units] In Commercial Distribution |
GS1 | 06924274953975 [Package] Contains: 06924274953968 Package: [10 Units] In Commercial Distribution |
GS1 | 06924274953982 [Package] Contains: 06924274953975 Package: [10 Units] In Commercial Distribution |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2016-11-14 |