MaxForce™
GUDID 08714729097099
Balloon Dilatation Catheter
BOSTON SCIENTIFIC CORPORATION
Gastrointestinal/biliary dilation balloon catheter, non-medicated| Primary Device ID | 08714729097099 |
| NIH Device Record Key | 4e430e90-e1b6-455e-8626-b2bed0a9e68f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MaxForce™ |
| Version Model Number | M00567420 |
| Company DUNS | 021717889 |
| Company Name | BOSTON SCIENTIFIC CORPORATION |
| 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 Dimensions
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08714729097099 [Primary] |
FDA Product Code
| FGE | CATHETER, BILIARY, DIAGNOSTIC |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2024-12-23 |
| Device Publish Date | 2015-09-24 |
On-Brand Devices [MaxForce™]
| 08714729097099 | Balloon Dilatation Catheter |
| 08714729097082 | Balloon Dilatation Catheter |
| 08714729097075 | Balloon Dilatation Catheter |
| 08714729097068 | Balloon Dilatation Catheter |
| 08714729097051 | Balloon Dilatation Catheter |
| 08714729097037 | Balloon Dilatation Catheter |
Trademark Results [MaxForce]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MAXFORCE 88289203 not registered Live/Pending |
Town & Country Linen Corp. 2019-02-05 |
 MAXFORCE 87604442 not registered Dead/Abandoned |
Power-to-Power Systems, LLC 2017-09-12 |
 MAXFORCE 87481043 5426341 Live/Registered |
Attack Mats, LLC 2017-06-08 |
 MAXFORCE 86797549 not registered Dead/Abandoned |
R1 Concepts Inc. 2015-10-23 |
 MAXFORCE 86652173 not registered Dead/Abandoned |
Bond Manufacturing, Co. 2015-06-04 |
 MAXFORCE 85156858 4075098 Live/Registered |
AMERICAN ROOF, INC. 2010-10-20 |
 MAXFORCE 78947441 3497263 Live/Registered |
Halliburton Energy Services, Inc. 2006-08-08 |
 MAXFORCE 78334080 not registered Dead/Abandoned |
Balcan Plastics Limited/Les Plastiques Balcan Limitee 2003-11-28 |
 MAXFORCE 78333168 not registered Dead/Abandoned |
Balcan Plastics Limited/Les Plastiques Balcan Limitee 2003-11-25 |
 MAXFORCE 77695937 3880707 Live/Registered |
MORAN FOODS, LLC 2009-03-20 |
 MAXFORCE 76707082 4161476 Live/Registered |
ALLIED INTERNATIONAL LLC 2011-04-01 |
 MAXFORCE 76625322 3149284 Dead/Cancelled |
ANCHOR LAMINA AMERICA, INC. 2004-12-21 |
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