Primary Device ID | 20653405005497 |
NIH Device Record Key | 746ec8b0-4177-459f-84e3-6b1533083787 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hi-Fi |
Version Model Number | HL7000 |
Catalog Number | HL7000 |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
Device Count | 12 |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00653405005493 [Unit of Use] |
GS1 | 10653405005490 [Primary] |
GS1 | 20653405005497 [Package] Contains: 10653405005490 Package: Box [1 Units] In Commercial Distribution |
GAT | Suture, nonabsorbable, synthetic, polyethylene |
GFA | BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-10-21 |
Device Publish Date | 2021-10-13 |
20653405002045 | HiFi SUTURE WITH DOUBLE ARMED MENISCAL NEEDLES |
20653405005497 | Hi-Fi® Passing Loop |
20653405005480 | 2MM Hi-Fi® Tape White/Black |
20653405005473 | 2MM Hi-Fi® Tape Blue |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HI-FI 98606499 not registered Live/Pending |
Dengie Crops Limited 2024-06-18 |
HI-FI 90103108 not registered Live/Pending |
Detour Enterprises Inc 2020-08-10 |
HI-FI 88873476 not registered Live/Pending |
LO-FI BREWING LLC 2020-04-15 |
HI-FI 88324493 5942045 Live/Registered |
Boiler Room Industries, LLC 2019-03-04 |
HI-FI 87137308 5677479 Live/Registered |
Dengie Crops Limited 2016-08-12 |
HI-FI 86912874 not registered Dead/Abandoned |
Alan Yang 2016-02-19 |
HI-FI 86620068 5638221 Live/Registered |
Derek Lam Beauty LLC 2015-05-05 |
HI-FI 86334249 not registered Dead/Abandoned |
LIFE IN HI-FI, INC 2014-07-11 |
HI-FI 86334248 not registered Dead/Abandoned |
LIFE IN HI-FI, INC 2014-07-11 |
HI-FI 85872845 not registered Dead/Abandoned |
LIFE IN HI-FI, INC. 2013-03-11 |
HI-FI 85823906 not registered Dead/Abandoned |
PEACHFUZZ, INC. 2013-01-15 |
HI-FI 78722869 3331534 Live/Registered |
CONMED CORPORATION 2005-09-29 |