Primary Device ID | 00372217039020 |
NIH Device Record Key | 9a7b6614-13cf-41bc-98e6-d0d3d5d4334d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Procare Spacer chamber Child |
Version Model Number | 240501 |
Company DUNS | 081149273 |
Company Name | ARISE MEDICAL LLC |
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 | false |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00372217039020 [Primary] |
NVP | Holding Chambers, Direct Patient Interface |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-09-16 |
Device Publish Date | 2019-09-07 |
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