Primary Device ID | 00836462004184 |
NIH Device Record Key | a5015ce3-b240-4ba8-bf25-5cd9fce3a071 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HyperForm |
Version Model Number | 104-4470 |
Catalog Number | 104-4470 |
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 | false |
OTC Over-The-Counter | true |
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 | |
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 |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 7 Millimeter |
Outer Diameter | 4 Millimeter |
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 |
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 | 00836462004184 [Primary] |
MJN | Catheter, intravascular occluding, temporary |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-03-21 |
Device Publish Date | 2015-10-06 |
00836462004689 | Occlusion Balloon System |
00836462004665 | Occlusion Balloon System |
00836462004641 | Occlusion Balloon System |
00836462004627 | Occlusion Balloon System |
00836462004603 | Occlusion Balloon System |
00836462004207 | Occlusion Balloon System |
00836462004184 | Occlusion Balloon System |
00763000294328 | BALLOON SYSTEM 104-4770 V20 HYPERFORM |
00763000294298 | BALLOON SYSTEM 104-4715 V20 HYPERFORM |
00763000294267 | BALLOON SYSTEM 104-4470 V20 HYPERFORM |
00763000294236 | BALLOON SYSTEM 104-4420 V20 HYPERFORM |
00763000294205 | BALLOON SYSTEM 104-4415 V20 HYPERFORM |
00763000294175 | BALLOON SYSTEM 104-4370 V20 HYPERFORM |
00763000294144 | BALLOON SYSTEM 104-4153 V20 HYPERFORM |