Primary Device ID | 00709078004049 |
NIH Device Record Key | 59cfa642-b3de-4d32-9bf3-611c199730f3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Anapod |
Version Model Number | A2003-1 |
Company DUNS | 092673953 |
Company Name | WESTMED, INC. |
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 | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00709078004049 [Primary] |
BTT | Humidifier, Respiratory Gas, (Direct Patient Interface) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-12-24 |
Device Publish Date | 2018-05-16 |
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10709078001182 | Replacement Cable |
10709078001175 | Power Supply Cable |
00709078007071 | Refurbished Controller, Anapod Domestic w Mounting Bracket |
10709078007849 | Anapod Humi-Therm Heated and Hunidified Anesthesia Heated Pediatric 96" Circuit |
10709078007498 | Anapod Humi-Therm Heated and Humidified Anesthesia Breathing Circuit Expandable Up to 96" |