Primary Device ID | 20653405043529 |
NIH Device Record Key | f3231b58-829c-47d6-8350-0bc2c42aee35 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HYFRE-VAC II |
Version Model Number | 7-900-13 |
Catalog Number | 7-900-13 |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
Device Count | 5 |
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 | false |
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 | 00653405043525 [Unit of Use] |
GS1 | 20653405043529 [Package] Contains: 30653405043526 Package: CARTON [5 Units] In Commercial Distribution |
GS1 | 30653405043526 [Primary] |
FYD | APPARATUS, EXHAUST, SURGICAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-10-21 |
Device Publish Date | 2016-09-24 |
20653405043529 | HYFRE-VAC II SMOKE EVACUATION SYSTEM, HAND HELD TUBING SET |
20653405043512 | HYFRE-VAC II SMOKE EVACUATION SYSTEM, FILTER |