Primary Device ID | 00836462016163 |
NIH Device Record Key | a4366215-48f9-42f4-a3b2-7879162076b6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Solitaire FR |
Version Model Number | SFR-6-30 |
Catalog Number | SFR-6-30 |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com |
Device Size Text, specify | 0 |
Length | 42 Millimeter |
Outer Diameter | 6 Millimeter |
Device Size Text, specify | 0 |
Length | 42 Millimeter |
Outer Diameter | 6 Millimeter |
Device Size Text, specify | 0 |
Length | 42 Millimeter |
Outer Diameter | 6 Millimeter |
Device Size Text, specify | 0 |
Length | 42 Millimeter |
Outer Diameter | 6 Millimeter |
Device Size Text, specify | 0 |
Length | 42 Millimeter |
Outer Diameter | 6 Millimeter |
Device Size Text, specify | 0 |
Length | 42 Millimeter |
Outer Diameter | 6 Millimeter |
Device Size Text, specify | 0 |
Length | 42 Millimeter |
Outer Diameter | 6 Millimeter |
Device Size Text, specify | 0 |
Length | 42 Millimeter |
Outer Diameter | 6 Millimeter |
Device Size Text, specify | 0 |
Length | 42 Millimeter |
Outer Diameter | 6 Millimeter |
Device Size Text, specify | 0 |
Length | 42 Millimeter |
Outer Diameter | 6 Millimeter |
Device Size Text, specify | 0 |
Length | 42 Millimeter |
Outer Diameter | 6 Millimeter |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00836462016163 [Primary] |
NRY | CATHETER, THROMBUS RETRIEVER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-23 |
00836462016163 | Revascularization Device |
00836462016156 | Revascularization Device |
00836462016149 | Revascularization Device |
00836462016132 | Revascularization Device |