Primary Device ID | 09420012416063 |
NIH Device Record Key | 86ace67f-f464-4ba1-810a-9b4bfd53a775 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fisher & Paykel Healthcare |
Version Model Number | RT241 |
Catalog Number | RT241 |
Company DUNS | 590153276 |
Company Name | FISHER & PAYKEL HEALTHCARE LIMITED |
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 | true |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 09420012416063 [Package] Contains: 09420012432162 Package: PACK [10 Units] In Commercial Distribution |
GS1 | 09420012432162 [Primary] |
BZE | Heater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-10 |
Device Publish Date | 2022-08-02 |
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