Primary Device ID | 00857326005079 |
NIH Device Record Key | f689731c-9565-493f-a0cc-04ffa9907512 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | XprESS ENT Dilation System |
Version Model Number | MSB |
Catalog Number | JD-206 |
Company DUNS | 017283879 |
Company Name | ENTELLUS MEDICAL, INC. |
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 | false |
Expiration Date | true |
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 | 00857326005079 [Primary] |
LRC | Instrument, Ent Manual Surgical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-06-07 |
Device Publish Date | 2017-11-27 |
00857326005147 | XprESS Ultra 6x8mm ENT Dilation System |
00857326005130 | XprESS Ultra 5x8mm ENT Dilation System |
00857326005123 | XprESS Ultra 6x20mm ENT Dilation System |
00857326005116 | XprESS Ultra 5x20mm ENT Dilation System |
00857326005079 | XprESS Pro 6x8mm ENT Dilation System |
00857326005062 | XprESS Pro 7x18mm ENT Dilation System |
00857326005055 | XprESS Pro 6x18mm ENT Dilation System |
00857326005048 | XprESS LoProfile 6x8mm ENTDilation System |
00857326005031 | XprESS LoProfile 5x8mm ENT Dilation System |
00857326005024 | XprESS LoProfile 7x20mm ENT Dilation System |
00857326005017 | XprESS LoProfile 6x20mm ENT Dilation System |
00857326005000 | XprESS LoProfile 5x20mm ENT Dilation System |