Primary Device ID | 10817170020090 |
NIH Device Record Key | dd348226-e197-4b87-ae1f-02cd7789567b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Nimbus II Flex |
Version Model Number | Nimbus II Flex |
Company DUNS | 079821136 |
Company Name | INFUTRONIX LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
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 | 00817170020093 [Primary] |
GS1 | 10817170020090 [Package] Contains: 00817170020093 Package: Inner pack [27 Units] In Commercial Distribution |
GS1 | 20817170020097 [Package] Contains: 00817170020093 Package: Case [60 Units] In Commercial Distribution |
MEA | Pump, Infusion, Pca |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-07-05 |
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10817170020083 - Nimbus II PainPRO | 2018-10-29 Ambulatory infusion pump |
40817170020046 - Nimbus | 2018-07-06 Administration set |
10817170020090 - Nimbus II Flex | 2018-07-06Ambulatory infusion pump |
10817170020090 - Nimbus II Flex | 2018-07-06 Ambulatory infusion pump |
10817170020106 - Nimbus | 2018-07-06 Ambulaotry infusion pump |
10817170020007 - Nimbus | 2018-03-29 Ambulatory infusion pump |