Primary Device ID | 06924274920199 |
NIH Device Record Key | a634d3f1-04ec-48d6-8681-604fb8d11648 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Disposable Grounding Pad Series |
Version Model Number | SY-SW3 |
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 | 06924274920199 [Primary] |
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 | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-03-10 |
06924274955405 | SY-MW4 |
06924274955351 | SY-M4 |
06924274951780 | P4500 |
06924274930099 | SY-C2 |
06924274930082 | SY-C1 |
06924274920243 | SY-BW4 |
06924274920236 | SY-BW3 |
6924274921004 | SY-BW2 |
06924274920212 | SY-BW1 |
06924274920205 | SY-SW4 |
06924274920199 | SY-SW3 |
6924274920854 | SY-SW2 |
6924274920809 | SY-SW1 |
6924274920601 | SY-MW3 |
6924274920557 | SY-MW2 |
6924274920502 | SY-MW1 |
06924274920120 | SY-B4 |
06924274920113 | SY-B3 |
6924274920953 | SY-B2 |
6924274920908 | SY-B1 |
06924274920083 | SY-S4 |
06924274920076 | SY-S3 |
6924274920755 | SY-S2 |
6924274920700 | SY-S1 |
6924274920403 | SY-M3 |
6924274920359 | SY-M2 |
6924274920304 | SY-M1 |