Primary Device ID | 20681490049157 |
NIH Device Record Key | bc8a972b-7639-4bba-b026-ad356e32a60c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FeatherTouch® |
Version Model Number | 1895524 |
Company DUNS | 835465063 |
Company Name | MEDTRONIC XOMED, 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 | 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 | 00681490049153 [Primary] |
GS1 | 20681490049157 [Package] Contains: 00681490049153 Package: PK [10 Units] In Commercial Distribution |
HRX | ARTHROSCOPE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-10-07 |
Device Publish Date | 2016-04-17 |
20681490051532 | RASP 1992210 FEATHERTOUCH 2PK FINE |
20681490051525 | RASP 1992208 FEATHERTOUCH 2PK COARSE |
00681490051095 | TRAY 1922006 FEATHERTOUCH STERILIZATION |
00681490051088 | CONVERTER 1922005 FEATHERTOUCH AUTO RASP |
20681490049157 | TUBING 1895524 10PK FEATHERTOUCH SUCTION |