Primary Device ID | 35099169457332 |
NIH Device Record Key | 255c1260-db47-494c-b93a-1d3a717a18a4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AIM |
Version Model Number | 4500 |
Company DUNS | 219683489 |
Company Name | VITALOGRAPH (IRELAND) 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 | 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 | false |
OTC Over-The-Counter | false |
Storage Environment Humidity | Between 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
Storage Environment Humidity | Between 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05099169457331 [Package] Contains: 15099169457338 Package: [1 Units] In Commercial Distribution |
GS1 | 15099169457338 [Primary] |
GS1 | 35099169457332 [Package] Contains: 05099169457331 Package: [25 Units] In Commercial Distribution |
BWF | SPIROMETER, THERAPEUTIC (INCENTIVE) |
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 | 2017-02-21 |
35099169457394 | 45739 |
35099169457387 | 45738 |
05099169457379 | 45737 |
05099169457355 | 45735 |
35099169457349 | 45734 |
35099169457332 | 45733 |
35099169457325 | 45732 |
35099169457103 | 45710 |
05099169331884 | Vitalograph AIM |