Primary Device ID | 00195278022646 |
NIH Device Record Key | 26617ab2-9e69-4ff7-a35f-13a5874ee2f2 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 5514182 Gas exhaust line, white conical |
Company DUNS | 401966697 |
Company Name | GE Healthcare Finland Oy |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
Expiration Date | false |
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 | 00195278022646 [Primary] |
CAI | Circuit, breathing (w connector, adaptor, y piece) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-02-17 |
Device Publish Date | 2022-02-09 |
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