Primary Device ID | 00868438000234 |
NIH Device Record Key | b6cb251e-e480-43fe-8ba6-beaac883d3c1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ClariFix |
Version Model Number | CFX-1000 |
Catalog Number | CFX-1000 |
Company DUNS | 079807364 |
Company Name | ARRINEX, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | 00868438000234 [Primary] |
GEH | Unit, Cryosurgical, Accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-12-10 |
Device Publish Date | 2019-12-02 |
00868438000227 | Cryogen Canister, 10ml |
00868438000210 | Cryogen Canister, 21ml |
00868438000203 | Cryotherapy Device |
00868438000258 | Cryogen Canister |
00868438000234 | Cryotherapy System |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CLARIFIX 86947753 5196955 Live/Registered |
Arrinex, Inc. 2016-03-21 |