Primary Device ID | 80841436114963 |
NIH Device Record Key | 3c50a9e4-a9a4-4250-be09-e83542e354b0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ultrasound Pad |
Version Model Number | H2O-007 |
Catalog Number | H2O-007 |
Company DUNS | 134614411 |
Company Name | CIVCO MEDICAL INSTRUMENTS CO., INC. |
Device Count | 100 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com | |
Phone | +1(319)248-6502 |
regulatory@civco.com |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep Away from Sunlight |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841436114967 [Primary] |
GS1 | 80841436114963 [Unit of Use] |
ITX | Transducer, ultrasonic, diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-07-01 |
Device Publish Date | 2021-06-23 |
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