Primary Device ID | 06924274952039 |
NIH Device Record Key | 59f172a9-96f7-4b32-97a6-f82683fab481 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Disposable Electrode Serie |
Version Model Number | P0013M |
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 | 06924274952008 [Primary] |
GS1 | 06924274952015 [Package] Contains: 06924274952008 Package: [12 Units] In Commercial Distribution |
GS1 | 06924274952022 [Package] Contains: 06924274952015 Package: [40 Units] In Commercial Distribution |
GS1 | 06924274952039 [Package] Contains: 06924274952022 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 |