Primary Device ID | 00763000299439 |
NIH Device Record Key | 00fe5b6c-2cb7-4c40-a463-4c99c69394ee |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Riptide™ |
Version Model Number | MAT-110-110 |
Company DUNS | 826110710 |
Company Name | Micro Therapeutics, Inc. |
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 | false |
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 | 00763000299439 [Primary] |
NRY | CATHETER, THROMBUS RETRIEVER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-01 |
Device Publish Date | 2020-08-24 |
00847536029118 | ASPIRATION TUBING AT-88-110 V01 US |
00847536029101 | ASPIRATION PUMP MAP-1000 V01 US |
00847536029095 | CANISTER MAC-1200 V01 US |
00847536034839 | TUBING MAT-110-110 V01 |
00763000299439 | TUBING MAT-110-110 V04 NA RIPTIDE |
00763000299422 | CANISTER MAC-1200 V04 NA RIPTIDE |
00763000299415 | PUMP MAP-1000 V02 NA RIPTIDE |