Primary Device ID | 07333066000657 |
NIH Device Record Key | 42db5b8f-d227-428a-af9a-6babf2abd87c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Stop Solution |
Version Model Number | 34-2256-11 |
Catalog Number | 34-2256-11 |
Company DUNS | 354019424 |
Company Name | Phadia AB |
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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +469999999999 |
xx@xx.xx |
Storage Environment Temperature | Between 2 Degrees Celsius and 32 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07333066000657 [Package] Contains: 07333066019710 Package: [6 Units] In Commercial Distribution |
GS1 | 07333066019710 [Primary] |
DHB | System, test, radioallergosorbent (rast) immunological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-04-05 |
Device Publish Date | 2019-03-28 |
07333066012483 | Stop Solution |
07333066011523 | Stop Solution |
07333066000657 | Stop Solution |
07333066000459 | Stop Solution |