Primary Device ID | 08714729469582 |
NIH Device Record Key | 3aceb03a-5c5f-4f7a-a033-d19144dc8c28 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Navigator |
Version Model Number | M0062502030 |
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 Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08714729469582 [Package] Contains: 08714729751502 Package: [5 Units] In Commercial Distribution |
GS1 | 08714729751502 [Primary] |
KOD | CATHETER, UROLOGICAL |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-11-18 |
Device Publish Date | 2016-09-24 |
08714729469629 | Ureteral Access Sheath Set |
08714729469612 | Ureteral Access Sheath Set |
08714729469605 | Ureteral Access Sheath Set |
08714729469599 | Ureteral Access Sheath Set |
08714729469582 | Ureteral Access Sheath Set |
08714729470359 | Ureteral Access Sheath Set |
08714729469575 | Ureteral Access Sheath Set |
08714729430018 | Ureteral Access Sheath Set |
08714729429999 | Ureteral Access Sheath Set |
08714729429968 | Ureteral Access Sheath Set |
08714729429944 | Ureteral Access Sheath Set |
08714729429920 | Ureteral Access Sheath Set |