Primary Device ID | 10886874115968 |
NIH Device Record Key | 4ba3a105-919c-47a5-82fc-7a2efa8b3a29 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Flexision |
Version Model Number | 490103 |
Company DUNS | 938647021 |
Company Name | INTUITIVE SURGICAL, 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 | 00886874115961 [Primary] |
GS1 | 10886874115968 [Package] Contains: 00886874115961 Package: BOX [5 Units] In Commercial Distribution |
EOQ | Bronchoscope (flexible or rigid) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-03-02 |
Device Publish Date | 2019-03-21 |
10886874115975 | Biopsy Needle, 19G |
10886874115968 | Biopsy Needle, 21G |
10886874115951 | Biopsy Needle, 23G |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() FLEXISION 88408980 not registered Live/Pending |
Intuitive Surgical Operations, Inc. 2019-04-30 |