Primary Device ID | 00840682111263 |
NIH Device Record Key | 00715937-5116-41d8-a6db-f1cd325db4fb |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 6S-D |
Company DUNS | 391532137 |
Company Name | PARALLEL DESIGN |
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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Handling Environment Humidity | Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840682111263 [Primary] |
IYO | System, imaging, pulsed echo, ultrasonic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-01-18 |
Device Publish Date | 2016-07-15 |
00840682110976 - NA | 2019-01-18 |
00840682111157 - NA | 2019-01-18 |
00840682111263 - NA | 2019-01-18 |
00840682111263 - NA | 2019-01-18 |
00840682111416 - NA | 2019-01-18 |
00840682115346 - NA | 2019-01-18 |
00840682124355 - NA | 2019-01-18 |
00840682124768 - NA | 2019-01-18 |
00840682136075 - NA | 2018-11-02 |