Primary Device ID | 10857160006260 |
NIH Device Record Key | 1f8e0a5e-d25b-4659-b0bf-136ccd2c10bd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HAART |
Version Model Number | 200-25US |
Catalog Number | 200-25US |
Company DUNS | 012321281 |
Company Name | BIOSTABLE ENGINEERING & SCIENCE |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | 10857160006260 [Primary] |
PST | Aortic Annuloplasty Ring |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2021-02-05 |
Device Publish Date | 2017-09-27 |
10857160006307 | Aortic Annuloplasty Ring |
10857160006291 | Aortic Annuloplasty Ring |
10857160006284 | Aortic Annuloplasty Device |
10857160006277 | Aortic Annuloplasty Ring |
10857160006260 | Aortic Annuloplasty Device |
10857160006253 | Aortic Annuloplasty Device |
10857160006246 | Aortic Annuloplasty Device |
10857160006239 | Aortic Annuloplasty Ring |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HAART 78172481 2819695 Dead/Cancelled |
Haart Limited 2002-10-09 |
HAART 77679691 4257921 Live/Registered |
BioStable Science & Engineering, Inc. 2009-02-27 |