Primary Device ID | 10190302000321 |
NIH Device Record Key | 140cc7bf-6bae-4276-8867-2105938a3aa8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Rnase P Fast 384-Well Instrument Verification Plate |
Version Model Number | 4432500 |
Company DUNS | 628548377 |
Company Name | LIFE TECHNOLOGIES HOLDINGS PTE. LTD. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 |