Primary Device ID | 20845854600082 |
NIH Device Record Key | e5aca0c4-fd95-409f-a901-40c69e392be8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Smoke Shark III |
Version Model Number | SE03-220 |
Catalog Number | SE03-220 |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10845854600085 [Primary] |
GS1 | 20845854600082 [Direct Marking] |
FYD | APPARATUS, EXHAUST, SURGICAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-02-22 |
Device Publish Date | 2021-02-12 |
30845854600102 | 6 Hour Filter |
20845854600099 | Smoke Shark III Smoke Evacuator 100V-120V 50/60Hz |
20845854600082 | Smoke Shark III Smoke Evacuator 220V-240V 50/60Hz |