Primary Device ID | 20884450443099 |
NIH Device Record Key | df80cf8b-a6cd-4cda-97f0-8641d898e55d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Coaxial Introducer |
Version Model Number | 10884450443092 |
Catalog Number | PP1356/B |
Company DUNS | 184763290 |
Company Name | Merit Medical Systems, Inc. |
Device Count | 10 |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884450443095 [Unit of Use] |
GS1 | 10884450443092 [Primary] |
GS1 | 20884450443099 [Package] Contains: 10884450443092 Package: [18 Units] In Commercial Distribution |
GDF | GUIDE, NEEDLE, SURGICAL |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-11-05 |
Device Publish Date | 2021-10-28 |
20884450443143 | 10884450443146 |
20884450443105 | 10884450443108 |
20884450443082 | 10884450443085 |
20884450443150 | 10884450443153 |
20884450443099 | 10884450443092 |
20884450443204 | 10884450443207 |
20884450443228 | 10884450443221 |
20884450443181 | 10884450443184 |