Primary Device ID | 10860327000278 |
NIH Device Record Key | b33065ad-290b-440c-81b0-cacfa4d3f997 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MicroTaper™ NV Non-Vascular Safety Introducer Set |
Version Model Number | SA-15-G100-NT-MT |
Company DUNS | 021348782 |
Company Name | SUMMIT ACCESS LLC |
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 Issuing Agency | Device ID |
---|---|
GS1 | 10860327000278 [Primary] |
KGZ | Accessories, Catheter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-13 |
Device Publish Date | 2022-10-05 |
10860327000292 | SA-15-G100-NT-ST |
10860327000285 | SA-15-G100-NT |
10860327000278 | SA-15-G100-NT-MT |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MICROTAPER 73530402 1362185 Live/Registered |
BRUNSWICK CORPORATION 1985-04-03 |