Primary Device ID | 08714729080602 |
NIH Device Record Key | a711afde-1eed-486d-8c40-eb67ab24cf5a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MaxForce TTS |
Version Model Number | M00589140 |
Company DUNS | 021717889 |
Company Name | BOSTON SCIENTIFIC CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 Issuing Agency | Device ID |
---|---|
GS1 | 08714729080602 [Primary] |
KNQ | Dilator, esophageal |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2024-12-23 |
Device Publish Date | 2016-09-24 |
08714729099925 | High Performance Balloon Dilatation Catheter |
08714729099918 | High Performance Balloon Dilatation Catheter |
08714729099901 | High Performance Balloon Dilatation Catheter |
08714729099895 | High Performance Balloon Dilatation Catheter |
08714729099598 | High Performance Balloon Dilatation Catheter |
08714729099581 | High Performance Balloon Dilatation Catheter |
08714729080619 | High Performance Balloon Dilatation Catheter |
08714729080602 | High Performance Balloon Dilatation Catheter |