Primary Device ID | B293HFT1100 |
NIH Device Record Key | c147efa2-586d-496b-91db-e810954c98a2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MIVI High Flow Tubing |
Version Model Number | HFT110 |
Company DUNS | 076836823 |
Company Name | MIVI NEUROVASCULAR |
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 |
Length | 112 Inch |
Length | 112 Inch |
Length | 112 Inch |
Length | 112 Inch |
Lumen/Inner Diameter | 0.11 Inch |
Length | 112 Inch |
Lumen/Inner Diameter | 0.11 Inch |
Length | 112 Inch |
Lumen/Inner Diameter | 0.11 Inch |
Length | 112 Inch |
Lumen/Inner Diameter | 0.11 Inch |
Length | 112 Inch |
Lumen/Inner Diameter | 0.11 Inch |
Length | 112 Inch |
Lumen/Inner Diameter | 0.11 Inch |
Length | 112 Inch |
Lumen/Inner Diameter | 0.11 Inch |
Length | 112 Inch |
Lumen/Inner Diameter | 0.11 Inch |
Length | 112 Inch |
Lumen/Inner Diameter | 0.11 Inch |
Length | 112 Inch |
Lumen/Inner Diameter | 0.11 Inch |
Length | 112 Inch |
Lumen/Inner Diameter | 0.11 Inch |
Length | 112 Inch |
Lumen/Inner Diameter | 0.11 Inch |
Length | 112 Inch |
Lumen/Inner Diameter | 0.11 Inch |
Length | 112 Inch |
Lumen/Inner Diameter | 0.11 Inch |
Length | 112 Inch |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B293HFT1100 [Primary] |
BYY | Tube, Aspirating, Flexible, Connecting |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-10-07 |
Device Publish Date | 2017-01-05 |
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